A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10061



Internal ID15542736
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:80151344..80183703hg38UCSC Ensembl
Outerchr1:80617029..80649388hg19UCSC Ensembl
Outerchr1:80389617..80421976hg18UCSC Ensembl
Outerchr1:80329050..80361409hg17UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg387152
hg197152
hg187152
hg177152
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1610
Supporting Variants
SamplesNA18956
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)nssv10061
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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