A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3531604



Internal ID18829885
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:45356841..45546503hg38UCSC Ensembl
Innerchr14:45826044..46015706hg19UCSC Ensembl
Innerchr14:44895794..45085456hg18UCSC Ensembl
Cytoband14q21.2
Allele length
AssemblyAllele length
hg38189663
hg19189663
hg18189663
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1048492
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)nssv3531604
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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