A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3883



Internal ID15548537
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:75391776..75422999hg38UCSC Ensembl
Outerchr3:75440927..75472150hg19UCSC Ensembl
Outerchr3:75523617..75554840hg18UCSC Ensembl
Outerchr3:75523617..75554840hg17UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg3811729
hg1911729
hg1811729
hg1711729
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7013, nssv3177, nssv309, nssv11063, nssv10352, nssv2401, nssv5975
SamplesNA12156, NA12878, NA18956, NA15510, NA18555, NA19240, NA19129
Known GenesFAM86DP
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)nsv3883
Frequency
Sample Size9
Observed Gain7
Observed Loss0
Observed Complex0
Frequencyn/a


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