A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv654800



Internal ID15391452
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:31851236..31915943hg38UCSC Ensembl
Innerchr12:32004170..32068877hg19UCSC Ensembl
Innerchr12:31895437..31960144hg18UCSC Ensembl
Innerchr12:31895437..31960144hg17UCSC Ensembl
Cytoband12p11.21
Allele length
AssemblyAllele length
hg3864708
hg1964708
hg1864708
hg1764708
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)nssv654800
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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