A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv665662



Internal ID15055628
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:963886..968910hg38UCSC Ensembl
Innerchr12:1073052..1078076hg19UCSC Ensembl
Innerchr12:943313..948337hg18UCSC Ensembl
Innerchr12:943313..948337hg17UCSC Ensembl
Cytoband12p13.33
Allele length
AssemblyAllele length
hg385025
hg195025
hg185025
hg175025
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516003
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv665662
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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