A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv703840



Internal ID15093806
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:9098005..9282648hg38UCSC Ensembl
Innerchr12:9250601..9435244hg19UCSC Ensembl
Innerchr12:9141868..9326511hg18UCSC Ensembl
Innerchr12:9141868..9326511hg17UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg38184644
hg19184644
hg18184644
hg17184644
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv527404
Supporting Variants
Samples
Known GenesA2M, A2MP1, LINC00987, MIR1244-1, MIR1244-2, MIR1244-3, PZP
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv703840
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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