A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv703997



Internal ID15093963
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:21414859..21415117hg38UCSC Ensembl
Innerchr12:21567793..21568051hg19UCSC Ensembl
Innerchr12:21459060..21459318hg18UCSC Ensembl
Innerchr12:21459060..21459318hg17UCSC Ensembl
Cytoband12p12.1
Allele length
AssemblyAllele length
hg38259
hg19259
hg18259
hg17259
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519603
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv703997
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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