A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv668347



Internal ID15058313
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:31113353..31256645hg38UCSC Ensembl
Innerchr12:31266287..31409579hg19UCSC Ensembl
Innerchr12:31157554..31300846hg18UCSC Ensembl
Innerchr12:31157554..31300846hg17UCSC Ensembl
Cytoband12p11.21
Allele length
AssemblyAllele length
hg38143293
hg19143293
hg18143293
hg17143293
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515974
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv668347
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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