A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2668555



Internal ID9934660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:129249547..129249719hg38UCSC Ensembl
chr10:131047811..131047983hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38173
hg19173
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6381136, essv6128080, essv5515134, essv5706678, essv6565529, essv6556043, essv5817021, essv6322077, essv6374270, essv5643135, essv5458501, essv6479615, essv5397007, essv5683245, essv6466700, essv6269713, essv5823616, essv6413999, essv5495906, essv6508918, essv5622921, essv5400939, essv6020271, essv6438296, essv5590344, essv6116568
SamplesNA19397, HG01462, HG01359, HG01374, HG01351, HG00689, HG01365, HG01440, NA19002, HG00739, NA18614, HG00149, NA19082, HG00653, HG01149, HG00740, NA18626, NA20581, HG00276, NA19390, HG00353, NA19444, HG01174, HG01137, HG00372, HG01125
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2668555
Frequency
Sample Size1151
Observed Gain0
Observed Loss26
Observed Complex0
Frequencyn/a


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