A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv8622



Internal ID15188556
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:83820688..83865527hg38UCSC Ensembl
Outerchr9:86435603..86480442hg19UCSC Ensembl
Outerchr9:85625423..85670262hg18UCSC Ensembl
Outerchr9:83665157..83709996hg17UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg3844840
hg1944840
hg1844840
hg1744840
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6590
Supporting Variants
SamplesNA12156
Known GenesKIF27
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)nssv8622
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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