A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3530768



Internal ID18482363
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:20884940..20934425hg38UCSC Ensembl
Innerchr14:21353099..21402584hg19UCSC Ensembl
Innerchr14:20422939..20472424hg18UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg3849486
hg1949486
hg1849486
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1053464
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)nssv3530768
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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