A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv667421



Internal ID15057387
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:122859474..122879651hg38UCSC Ensembl
Innerchr12:123344021..123364198hg19UCSC Ensembl
Innerchr12:121909974..121930151hg18UCSC Ensembl
Innerchr12:121868901..121889078hg17UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg3820178
hg1920178
hg1820178
hg1720178
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517200
Supporting Variants
Samples
Known GenesHIP1R, VPS37B
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv667421
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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