A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv687654



Internal ID15077620
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:92865431..92867251hg38UCSC Ensembl
Innerchr6:93575149..93576969hg19UCSC Ensembl
Innerchr6:93631870..93633690hg18UCSC Ensembl
Innerchr6:93631870..93633690hg17UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg381821
hg191821
hg181821
hg171821
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)nssv687654
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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