A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3644



Internal ID15191686
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:42307213..42338738hg38UCSC Ensembl
Outerchr8:42164731..42196256hg19UCSC Ensembl
Outerchr8:42283888..42315413hg18UCSC Ensembl
Outerchr8:42283888..42315413hg17UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg3831526
hg1931526
hg1831526
hg1731526
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6169
Supporting Variants
SamplesNA12878
Known GenesIKBKB, POLB
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)nssv3644
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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