A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9631



Internal ID15540172
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:162790511..162936799hg38UCSC Ensembl
Outerchr3:162508299..162654587hg19UCSC Ensembl
Outerchr3:163990993..164137281hg18UCSC Ensembl
Outerchr3:163991001..164137289hg17UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg38146289
hg19146289
hg18146289
hg17146289
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4093
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)nssv9631
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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