A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3958



Internal ID15548619
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:116481123..116505591hg38UCSC Ensembl
Outerchr3:116199970..116224438hg19UCSC Ensembl
Outerchr3:117682660..117707128hg18UCSC Ensembl
Outerchr3:117682660..117707128hg17UCSC Ensembl
Cytoband3q13.31
Allele length
AssemblyAllele length
hg3824469
hg1924469
hg1824469
hg1724469
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv9623
SamplesNA18507
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)nsv3958
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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