A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9566



Internal ID15539748
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:110826246..110849488hg38UCSC Ensembl
Outerchr1:111368868..111392110hg19UCSC Ensembl
Outerchr1:111170391..111193633hg18UCSC Ensembl
Outerchr1:111080910..111104152hg17UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg3823243
hg1923243
hg1823243
hg1723243
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv2387
Supporting Variants
SamplesNA18507
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)nssv9566
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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