A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4324



Internal ID15202336
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 StatusM
Merged Variants
Supporting Variantsnssv4739
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)nsv4324
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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