A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3633240



Internal ID6673362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:95185612..95186267hg38UCSC Ensembl
Innerchr13:95185618..95186262hg38UCSC Ensembl
Outerchr13:95185607..95186273hg38UCSC Ensembl
chr13:95837866..95838521hg19UCSC Ensembl
Innerchr13:95837872..95838516hg19UCSC Ensembl
Outerchr13:95837861..95838527hg19UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg38656
hg19656
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14868839, essv14868847, essv14868842, essv14868849, essv14868848, essv14868846, essv14868833, essv14868841, essv14868843, essv14868836, essv14868838, essv14868840, essv14868844, essv14868835, essv14868845, essv14868834, essv14868837
SamplesNA19026, NA19310, HG03066, HG03295, HG02419, NA19144, HG03109, HG02973, NA19028, NA20356, HG02009, HG02461, HG01894, HG03061, HG02628, NA19385, HG03082
Known GenesABCC4
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3633240
Frequency
Sample Size2504
Observed Gain0
Observed Loss17
Observed Complex0
Frequencyn/a


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