A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6294



Internal ID15537569
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:120082165..120127564hg38UCSC Ensembl
Outerchr9:122844443..122889842hg19UCSC Ensembl
Outerchr9:121884264..121929663hg18UCSC Ensembl
Outerchr9:119923997..119969396hg17UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg3845400
hg1945400
hg1845400
hg1745400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6697
Supporting Variants
SamplesNA12156
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)nssv6294
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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