A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6495



Internal ID15551410
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:18529851..18563944hg38UCSC Ensembl
Outerchr9:18529849..18563942hg19UCSC Ensembl
Outerchr9:18519849..18553942hg18UCSC Ensembl
Outerchr9:18519849..18553942hg17UCSC Ensembl
Cytoband9p22.1
Allele length
AssemblyAllele length
hg385935
hg195935
hg185935
hg175935
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2805
SamplesNA18555
Known GenesADAMTSL1
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)nsv6495
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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