A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3531633



Internal ID18829914
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:45356841..45555776hg38UCSC Ensembl
Innerchr14:45826044..46024979hg19UCSC Ensembl
Innerchr14:44895794..45094729hg18UCSC Ensembl
Cytoband14q21.2
Allele length
AssemblyAllele length
hg38198936
hg19198936
hg18198936
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1043014
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)nssv3531633
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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