A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv696300



Internal ID15432952
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:42604069..42673966hg38UCSC Ensembl
Innerchr6:42571807..42641704hg19UCSC Ensembl
Innerchr6:42679785..42749682hg18UCSC Ensembl
Innerchr6:42679785..42749682hg17UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg3869898
hg1969898
hg1869898
hg1769898
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv518847
Supporting Variants
Samples
Known GenesUBR2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv696300
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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