A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3612499



Internal ID6999400
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:20988181..20991799hg38UCSC Ensembl
Innerchr7:20988206..20991775hg38UCSC Ensembl
Outerchr7:20988157..20991824hg38UCSC Ensembl
chr7:21027800..21031418hg19UCSC Ensembl
Innerchr7:21027825..21031394hg19UCSC Ensembl
Outerchr7:21027776..21031443hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg383619
hg193619
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12693654
SamplesNA18748
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3612499
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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