A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3712549



Internal ID19010830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:73283037..73344035hg38UCSC Ensembl
Innerchr12:73676817..73737815hg19UCSC Ensembl
Innerchr12:71963084..72024082hg18UCSC Ensembl
Cytoband12q21.1
Allele length
AssemblyAllele length
hg3860999
hg1960999
hg1860999
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1036829
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)nssv3712549
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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