A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3615067



Internal ID7001956
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:133326980..133329494hg38UCSC Ensembl
Innerchr7:133326980..133329494hg38UCSC Ensembl
Outerchr7:133326900..133329584hg38UCSC Ensembl
chr7:133011734..133014248hg19UCSC Ensembl
Innerchr7:133011734..133014248hg19UCSC Ensembl
Outerchr7:133011654..133014338hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg382515
hg192515
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12973594, essv12973595
SamplesNA19701, NA19379
Known GenesEXOC4
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3615067
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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