A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6539



Internal ID15551458
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:38574433..38608187hg38UCSC Ensembl
Outerchr9:38574430..38608184hg19UCSC Ensembl
Outerchr9:38564430..38598184hg18UCSC Ensembl
Outerchr9:38564430..38598184hg17UCSC Ensembl
Cytoband9p13.1
Allele length
AssemblyAllele length
hg386272
hg196272
hg186272
hg176272
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2807
SamplesNA18555
Known GenesANKRD18A
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)nsv6539
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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