A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6547



Internal ID15551467
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:68232525..68266957hg38UCSC Ensembl
Outerchr9:70847441..70881873hg19UCSC Ensembl
Outerchr9:70037261..70071693hg18UCSC Ensembl
Outerchr9:68076995..68111427hg17UCSC Ensembl
Cytoband9q13
Allele length
AssemblyAllele length
hg385598
hg195598
hg185598
hg175598
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2810
SamplesNA18555
Known GenesCBWD3, CBWD5
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)nsv6547
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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