A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv678058



Internal ID15068024
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:92865431..92867774hg38UCSC Ensembl
Innerchr6:93575149..93577492hg19UCSC Ensembl
Innerchr6:93631870..93634213hg18UCSC Ensembl
Innerchr6:93631870..93634213hg17UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg382344
hg192344
hg182344
hg172344
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517329
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv678058
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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