A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9324



Internal ID15540275
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:110831741..110850437hg38UCSC Ensembl
Outerchr1:111374363..111393059hg19UCSC Ensembl
Outerchr1:111175886..111194582hg18UCSC Ensembl
Outerchr1:111086405..111105101hg17UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg3818697
hg1918697
hg1818697
hg1718697
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv2387
Supporting Variants
SamplesNA18517
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)nssv9324
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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