A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6690



Internal ID15551625
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:118008974..118043641hg38UCSC Ensembl
Outerchr9:120771252..120805919hg19UCSC Ensembl
Outerchr9:119811073..119845740hg18UCSC Ensembl
Outerchr9:117850806..117885473hg17UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg385354
hg195354
hg185354
hg175354
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2821
SamplesNA18555
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)nsv6690
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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