A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6693



Internal ID15551628
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:118985094..119018062hg38UCSC Ensembl
Outerchr9:121747372..121780340hg19UCSC Ensembl
Outerchr9:120787193..120820161hg18UCSC Ensembl
Outerchr9:118826926..118859894hg17UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg388018
hg198018
hg188018
hg178018
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv832
SamplesNA19240
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)nsv6693
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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