A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6537



Internal ID15551456
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:38422798..38456112hg38UCSC Ensembl
Outerchr9:38422795..38456109hg19UCSC Ensembl
Outerchr9:38412795..38446109hg18UCSC Ensembl
Outerchr9:38412795..38446109hg17UCSC Ensembl
Cytoband9p13.1
Allele length
AssemblyAllele length
hg387682
hg197682
hg187682
hg177682
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv799
SamplesNA19240
Known GenesIGFBPL1
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)nsv6537
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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