A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3532183



Internal ID18830464
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:22124657..22509792hg38UCSC Ensembl
Innerchr14:22592615..22978775hg19UCSC Ensembl
Innerchr14:21662455..22048615hg18UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38385136
hg19386161
hg18386161
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1051461
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)nssv3532183
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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