A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv8636



Internal ID15535228
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:96786505..96831686hg38UCSC Ensembl
Outerchr9:99548787..99593968hg19UCSC Ensembl
Outerchr9:98588608..98633789hg18UCSC Ensembl
Outerchr9:96628342..96673523hg17UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg3845182
hg1945182
hg1845182
hg1745182
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6624
Supporting Variants
SamplesNA12156
Known GenesZNF782
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)nssv8636
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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