A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1763



Internal ID15194360
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:96895704..96925153hg38UCSC Ensembl
Outerchr8:97907932..97937381hg19UCSC Ensembl
Outerchr8:97977108..98006557hg18UCSC Ensembl
Outerchr8:97977108..98006557hg17UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg3810572
hg1910572
hg1810572
hg1710572
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6324
Supporting Variants
SamplesNA18555
Known GenesCPQ
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)nssv1763
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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