A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv678579



Internal ID15068545
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:31392612..31409810hg38UCSC Ensembl
Innerchr6:31360389..31377587hg19UCSC Ensembl
Innerchr6:31468368..31485566hg18UCSC Ensembl
Innerchr6:31468368..31485566hg17UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3817199
hg1917199
hg1817199
hg1717199
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517441
Supporting Variants
Samples
Known GenesMICA
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv678579
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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