A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3530839



Internal ID18482434
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:20888085..20941810hg38UCSC Ensembl
Innerchr14:21356244..21409969hg19UCSC Ensembl
Innerchr14:20426084..20479809hg18UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg3853726
hg1953726
hg1853726
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1042584
Supporting Variants
Samples
Known GenesECRP, RNASE3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3530839
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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