A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9763



Internal ID15540085
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:38471177..38507221hg38UCSC Ensembl
Outerchr9:38471174..38507218hg19UCSC Ensembl
Outerchr9:38461174..38497218hg18UCSC Ensembl
Outerchr9:38461174..38497218hg17UCSC Ensembl
Cytoband9p13.1
Allele length
AssemblyAllele length
hg3836045
hg1936045
hg1836045
hg1736045
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv6538
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)nssv9763
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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