A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3615624



Internal ID7002513
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:155144281..155160500hg38UCSC Ensembl
Innerchr7:155144781..155160000hg38UCSC Ensembl
Outerchr7:155143281..155161500hg38UCSC Ensembl
chr7:154935991..154952210hg19UCSC Ensembl
Innerchr7:154936491..154951710hg19UCSC Ensembl
Outerchr7:154934991..154953210hg19UCSC Ensembl
Cytoband7q36.2
Allele length
AssemblyAllele length
hg3816220
hg1916220
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13033245, essv13033247, essv13033246
SamplesHG03394, HG03472, HG03084
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3615624
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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