A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2676428



Internal ID9942533
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:45836285..45836592hg38UCSC Ensembl
chrX:45695712..45696017hg19UCSC Ensembl
CytobandXp11.3
Allele length
AssemblyAllele length
hg38308
hg19306
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6594443, essv6017866, essv5523291, essv5878501, essv6062505, essv5814465, essv6083413, essv5581707, essv5633100, essv6386634, essv6184035, essv5760869, essv6591759, essv6418376, essv5546270, essv6486353, essv6534854, essv5608532, essv5861619, essv5977817
SamplesNA19397, HG01052, NA18507, NA19359, NA19355, NA19920, NA19746, NA19396, NA19235, NA19455, NA18871, NA19452, NA18523, NA19834, NA19108, NA18517, NA19311, HG01108, NA19818, NA19376
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2676428
Frequency
Sample Size1151
Observed Gain0
Observed Loss20
Observed Complex0
Frequencyn/a


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