A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3664



Internal ID15538392
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:85643198..85646540hg38UCSC Ensembl
Outerchr8:86555427..86558769hg19UCSC Ensembl
Outerchr8:86742679..86746021hg18UCSC Ensembl
Outerchr8:86742679..86746021hg17UCSC Ensembl
Cytoband8q21.2
Allele length
AssemblyAllele length
hg3821802
hg1921802
hg1821802
hg1721802
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6284
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)nssv3664
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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