A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6695



Internal ID15551630
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:119526499..119560860hg38UCSC Ensembl
Outerchr9:122288777..122323138hg19UCSC Ensembl
Outerchr9:121328598..121362959hg18UCSC Ensembl
Outerchr9:119368331..119402692hg17UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg3834362
hg1934362
hg1834362
hg1734362
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv9923
SamplesNA18507
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)nsv6695
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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