A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3523608



Internal ID18821889
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:58314825..58338272hg38UCSC Ensembl
Innerchr12:58708608..58732055hg19UCSC Ensembl
Innerchr12:56994875..57018322hg18UCSC Ensembl
Cytoband12q14.1
Allele length
AssemblyAllele length
hg3823448
hg1923448
hg1823448
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1035772
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3523608
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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