A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3532203



Internal ID18830484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:22147511..22490838hg38UCSC Ensembl
Innerchr14:22615465..22959826hg19UCSC Ensembl
Innerchr14:21685305..22029666hg18UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38343328
hg19344362
hg18344362
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1049042
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)nssv3532203
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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