A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6099



Internal ID15204288
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:24597662..24627801hg38UCSC Ensembl
Outerchr10:24886591..24916730hg19UCSC Ensembl
Outerchr10:24926597..24956736hg18UCSC Ensembl
Outerchr10:24926597..24956736hg17UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg389142
hg199142
hg189142
hg179142
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv5278
SamplesNA19129
Known GenesARHGAP21
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)nsv6099
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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