A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6496



Internal ID15551411
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:18586936..18609803hg38UCSC Ensembl
Outerchr9:18586934..18609801hg19UCSC Ensembl
Outerchr9:18576934..18599801hg18UCSC Ensembl
Outerchr9:18576934..18599801hg17UCSC Ensembl
Cytoband9p22.1
Allele length
AssemblyAllele length
hg3822868
hg1922868
hg1822868
hg1722868
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8590
SamplesNA12156
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)nsv6496
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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