A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2677707



Internal ID9597126
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:27753173..27753298hg38UCSC Ensembl
chr10:28042102..28042227hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg38126
hg19126
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5457231, essv5446221, essv5803688, essv5575240, essv5993256, essv5835454, essv5779246, essv6205877, essv6469250, essv5752614, essv6242887, essv6223977, essv6237436, essv6147840, essv5611843, essv6018237, essv6104091
SamplesHG00152, HG01250, HG00310, NA20299, NA19463, HG00096, HG01124, HG00149, HG00254, NA20589, NA12006, NA20769, NA19005, NA18941, HG01356, HG01060, HG00143
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2677707
Frequency
Sample Size1151
Observed Gain0
Observed Loss17
Observed Complex0
Frequencyn/a


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