A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3712281



Internal ID19010562
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:35432355..35536457hg38UCSC Ensembl
Innerchr14:35901561..36005663hg19UCSC Ensembl
Innerchr14:34971312..35075414hg18UCSC Ensembl
Cytoband14q13.2
Allele length
AssemblyAllele length
hg38104103
hg19104103
hg18104103
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1039975
Supporting Variants
Samples
Known GenesINSM2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3712281
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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