A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv700224



Internal ID15090190
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:150064339..150064750hg38UCSC Ensembl
Innerchr6:150385475..150385886hg19UCSC Ensembl
Innerchr6:150427168..150427579hg18UCSC Ensembl
Innerchr6:150477589..150478000hg17UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg38412
hg19412
hg18412
hg17412
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517022
Supporting Variants
Samples
Known GenesULBP3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv700224
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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