A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3713538



Internal ID19011819
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:84864200..85219978hg38UCSC Ensembl
Innerchr14:85330544..85686322hg19UCSC Ensembl
Innerchr14:84400297..84756075hg18UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg38355779
hg19355779
hg18355779
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1048026
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)nssv3713538
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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