A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695991



Internal ID15085957
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:127725568..127741682hg38UCSC Ensembl
Innerchr6:128046713..128062827hg19UCSC Ensembl
Innerchr6:128088406..128104520hg18UCSC Ensembl
Innerchr6:128088406..128104520hg17UCSC Ensembl
Cytoband6q22.33
Allele length
AssemblyAllele length
hg3816115
hg1916115
hg1816115
hg1716115
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv518548
Supporting Variants
Samples
Known GenesTHEMIS
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695991
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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