A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4886



Internal ID15202954
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:77085439..77118582hg38UCSC Ensembl
Outerchr5:76381264..76414407hg19UCSC Ensembl
Outerchr5:76417020..76450163hg18UCSC Ensembl
Outerchr5:76417020..76450163hg17UCSC Ensembl
Cytoband5q13.3
Allele length
AssemblyAllele length
hg386832
hg196832
hg186832
hg176832
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2526
SamplesNA18555
Known GenesZBED3, ZBED3-AS1
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)nsv4886
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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