A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2659431



Internal ID9925537
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:64950801..64954784hg38UCSC Ensembl
Outerchr15:64950424..64955145hg38UCSC Ensembl
Innerchr15:65243016..65247122hg19UCSC Ensembl
Outerchr15:65242645..65247492hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg384722
hg194848
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5762685, essv5517647, essv5518744, essv6526432, essv5716212, essv6280142, essv6117636, essv5969224, essv5921150, essv5742680, essv5725575, essv5996985, essv6297842, essv6068331, essv6488120, essv6222513, essv5713795, essv6556170, essv5549829, essv5817279, essv6061226, essv6301724, essv5798782, essv5672959, essv5465968, essv5557235, essv5907806, essv5890821, essv5502261, essv6125198
SamplesNA18502, NA18508, NA18507, NA18917, NA19190, NA18519, NA19131, NA19138, NA19130, NA18874, NA18868, NA19235, NA19207, NA19172, NA19159, NA19189, NA18520, NA19209, NA18908, NA18910, NA18856, NA18912, NA19160, NA19248, NA19093, NA18873, NA19116, NA19213, NA18505, NA18487
Known GenesANKDD1A
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2659431
Frequency
Sample Size1151
Observed Gain0
Observed Loss30
Observed Complex0
Frequencyn/a


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