A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3614650



Internal ID7001543
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:113496958..113508472hg38UCSC Ensembl
Innerchr7:113496958..113508472hg38UCSC Ensembl
Outerchr7:113496458..113508972hg38UCSC Ensembl
chr7:113137013..113148527hg19UCSC Ensembl
Innerchr7:113137013..113148527hg19UCSC Ensembl
Outerchr7:113136513..113149027hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg3811515
hg1911515
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12931477, essv12931475, essv12931476
SamplesHG03679, HG02690, NA20889
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3614650
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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