A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3524596



Internal ID18822877
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:66778169..66863655hg38UCSC Ensembl
Innerchr12:67171949..67257435hg19UCSC Ensembl
Innerchr12:65458216..65543702hg18UCSC Ensembl
Cytoband12q14.3
Allele length
AssemblyAllele length
hg3885487
hg1985487
hg1885487
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1042117
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)nssv3524596
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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