A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv652994



Internal ID15389646
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:31848581..31900901hg38UCSC Ensembl
Innerchr12:32001515..32053835hg19UCSC Ensembl
Innerchr12:31892782..31945102hg18UCSC Ensembl
Innerchr12:31892782..31945102hg17UCSC Ensembl
Cytoband12p11.21
Allele length
AssemblyAllele length
hg3852321
hg1952321
hg1852321
hg1752321
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516507
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv652994
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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