A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6635



Internal ID15551564
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:98965975..99010971hg38UCSC Ensembl
Outerchr9:101728257..101773253hg19UCSC Ensembl
Outerchr9:100768078..100813074hg18UCSC Ensembl
Outerchr9:98807812..98852808hg17UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg3844997
hg1944997
hg1844997
hg1744997
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8644
SamplesNA12156
Known GenesCOL15A1
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)nsv6635
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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