A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4015897



Internal ID22077528
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:141033022..141034092hg38UCSC Ensembl
Outerchr3:141029351..141036736hg38UCSC Ensembl
Innerchr3:140751864..140752934hg19UCSC Ensembl
Outerchr3:140748193..140755578hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg387386
hg197386
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1156021
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4015897
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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