A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2662425



Internal ID9928530
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:8206394..8229200hg38UCSC Ensembl
Outerchr8:8206023..8229570hg38UCSC Ensembl
Innerchr8:8063916..8086722hg19UCSC Ensembl
Outerchr8:8063545..8087092hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3823548
hg1923548
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1266e199
Supporting Variantsessv5513437, essv5520119, essv6247307, essv6126482, essv6125619, essv5775830, essv5782215, essv5595151, essv6537796, essv6272915, essv5739604, essv5671901, essv6203514, essv6372517, essv5708230, essv5613393, essv6428543, essv5581490, essv5834597, essv6501824, essv5777839, essv6364491, essv5886314, essv6530729, essv6181135, essv6109611, essv6272478, essv6480702, essv6576392, essv6054335, essv5939333, essv6237211, essv6381793, essv6384707, essv6303156, essv5659974, essv6249301, essv5550666, essv5797105, essv6137009, essv5980020, essv6590409, essv6193676, essv5793042, essv6276009, essv5457878, essv5411947, essv5767119
SamplesHG00361, HG00187, HG00315, HG00318, HG00179, HG00177, HG00327, HG00271, HG00173, HG00330, HG00346, HG00369, HG00270, HG00334, HG00281, HG00335, HG00325, HG00309, HG00182, HG00338, HG00326, HG00313, HG00188, HG00266, HG00176, HG00282, HG00328, HG00275, HG00284, HG00273, HG00331, HG00321, HG00336, HG00366, HG00375, HG00357, HG00319, HG00339, HG00269, HG00329, HG00342, HG00267, HG00186, HG00280, HG00343, HG00372, HG00345, HG00180
Known GenesFAM86B3P
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2662425
Frequency
Sample Size1151
Observed Gain0
Observed Loss48
Observed Complex0
Frequencyn/a


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