A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1012712



Internal ID19101929
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:186716473..186775954hg38UCSC Ensembl
Innerchr3:186434262..186493743hg19UCSC Ensembl
Innerchr3:187916956..187976437hg18UCSC Ensembl
Cytoband3q27.3
Allele length
AssemblyAllele length
hg3859482
hg1959482
hg1859482
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3615031
Samples
Known GenesKNG1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1012712
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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