A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3712431



Internal ID18664026
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:33710476..34701551hg38UCSC Ensembl
Innerchr12:33863411..34854486hg19UCSC Ensembl
Innerchr12:33754678..34745753hg18UCSC Ensembl
Cytoband12p11.1
Allele length
AssemblyAllele length
hg38991076
hg19991076
hg18991076
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1040812
Supporting Variants
Samples
Known GenesALG10
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3712431
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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