A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705489



Internal ID15442141
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:164208057..164210430hg38UCSC Ensembl
Innerchr6:164629089..164631462hg19UCSC Ensembl
Innerchr6:164549079..164551452hg18UCSC Ensembl
Innerchr6:164599500..164601873hg17UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg382374
hg192374
hg182374
hg172374
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv528815
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705489
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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