A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7506



Internal ID15205836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:97142683..97180452hg38UCSC Ensembl
Outerchr10:98902440..98940209hg19UCSC Ensembl
Outerchr10:98892430..98930199hg18UCSC Ensembl
Outerchr10:98892430..98930199hg17UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg3837770
hg1937770
hg1837770
hg1737770
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv6410
SamplesNA12156
Known GenesARHGAP19-SLIT1, SLIT1
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)nsv7506
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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