A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4361



Internal ID15539088
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:79456518..79484665hg38UCSC Ensembl
Outerchr1:79922203..79950350hg19UCSC Ensembl
Outerchr1:79694791..79722938hg18UCSC Ensembl
Outerchr1:79634224..79662371hg17UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3811589
hg1911589
hg1811589
hg1711589
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1599
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)nssv4361
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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