A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4739



Internal ID15196558
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:46996023..47029942hg38UCSC Ensembl
Outerchr4:46998040..47031959hg19UCSC Ensembl
Outerchr4:46692797..46726716hg18UCSC Ensembl
Outerchr4:46838968..46872887hg17UCSC Ensembl
Cytoband4p12
Allele length
AssemblyAllele length
hg385365
hg195365
hg185365
hg175365
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4324
Supporting Variants
SamplesNA19129
Known Genes
MethodSequencing
AnalysisEnd-sequence pairs were mapped to the human genome assembly (hg17) using a previously described algorithm (Tuzun et al 2005)
PlatformCapillary
Comments
ReferenceKidd_et_al_2008
Pubmed ID18451855
Accession Number(s)nssv4739
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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