A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3177



Internal ID15537905
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:75391776..75414956hg38UCSC Ensembl
Outerchr3:75440927..75464107hg19UCSC Ensembl
Outerchr3:75523617..75546797hg18UCSC Ensembl
Outerchr3:75523617..75546797hg17UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg389862
hg199862
hg189862
hg179862
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3883
Supporting Variants
SamplesNA12878
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)nssv3177
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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