A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv336



Internal ID15545114
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:144880383..144896509hg38UCSC Ensembl
Outerchr3:144599225..144615351hg19UCSC Ensembl
Outerchr3:146081915..146098041hg18UCSC Ensembl
Outerchr3:146081923..146098049hg17UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg387161
hg197161
hg187161
hg177161
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4044
Supporting Variants
SamplesNA19240
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)nssv336
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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