A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6696



Internal ID15551631
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:120029110..120074085hg38UCSC Ensembl
Outerchr9:122791388..122836363hg19UCSC Ensembl
Outerchr9:121831209..121876184hg18UCSC Ensembl
Outerchr9:119870942..119915917hg17UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg3844976
hg1944976
hg1844976
hg1744976
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8659
SamplesNA12156
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)nsv6696
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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