A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4386



Internal ID15549090
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:72993832..73026776hg38UCSC Ensembl
Outerchr4:73859549..73892493hg19UCSC Ensembl
Outerchr4:74078413..74111357hg18UCSC Ensembl
Outerchr4:74224584..74257528hg17UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg386496
hg196496
hg186496
hg176496
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7096
SamplesNA12156
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)nsv4386
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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