A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv704277



Internal ID15440929
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:32608624..32618978hg38UCSC Ensembl
Innerchr12:32761558..32771912hg19UCSC Ensembl
Innerchr12:32652825..32663179hg18UCSC Ensembl
Innerchr12:32652825..32663179hg17UCSC Ensembl
Cytoband12p11.21
Allele length
AssemblyAllele length
hg3810355
hg1910355
hg1810355
hg1710355
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv527786
Supporting Variants
Samples
Known GenesFGD4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv704277
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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