A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv657859



Internal ID15047825
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:21414859..21430308hg38UCSC Ensembl
Innerchr12:21567793..21583242hg19UCSC Ensembl
Innerchr12:21459060..21474509hg18UCSC Ensembl
Innerchr12:21459060..21474509hg17UCSC Ensembl
Cytoband12p12.1
Allele length
AssemblyAllele length
hg3815450
hg1915450
hg1815450
hg1715450
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
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)nssv657859
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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