A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6694



Internal ID15551629
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:119459862..119504578hg38UCSC Ensembl
Outerchr9:122222140..122266856hg19UCSC Ensembl
Outerchr9:121261961..121306677hg18UCSC Ensembl
Outerchr9:119301694..119346410hg17UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg3844717
hg1944717
hg1844717
hg1744717
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv5178
SamplesNA19129
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)nsv6694
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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