A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6680



Internal ID15551614
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:114928108..114937024hg38UCSC Ensembl
Outerchr9:117690388..117699304hg19UCSC Ensembl
Outerchr9:116730209..116739125hg18UCSC Ensembl
Outerchr9:114769942..114778858hg17UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg388917
hg198917
hg188917
hg178917
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8654
SamplesNA12156
Known GenesTNFSF8
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)nsv6680
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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