A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3615223



Internal ID7002112
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:140255522..140256878hg38UCSC Ensembl
Innerchr7:140255526..140256874hg38UCSC Ensembl
Outerchr7:140255518..140256882hg38UCSC Ensembl
chr7:139955322..139956678hg19UCSC Ensembl
Innerchr7:139955326..139956674hg19UCSC Ensembl
Outerchr7:139955318..139956682hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg381357
hg191357
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12983070
SamplesHG02348
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3615223
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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