A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4009461



Internal ID22071092
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:52034496..52037134hg38UCSC Ensembl
Outerchr14:52032648..52040711hg38UCSC Ensembl
Innerchr14:52501214..52503852hg19UCSC Ensembl
Outerchr14:52499366..52507429hg19UCSC Ensembl
Cytoband14q22.1
Allele length
AssemblyAllele length
hg388064
hg198064
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1155024
Supporting Variants
Samples
Known GenesNID2
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4009461
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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