A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv704113



Internal ID15094079
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:10482629..10488368hg38UCSC Ensembl
Innerchr6:10482862..10488601hg19UCSC Ensembl
Innerchr6:10590848..10596587hg18UCSC Ensembl
Innerchr6:10590848..10596587hg17UCSC Ensembl
Cytoband6p24.3
Allele length
AssemblyAllele length
hg385740
hg195740
hg185740
hg175740
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520598
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv704113
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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