A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9984



Internal ID15541901
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:25810460..25813604hg38UCSC Ensembl
Outerchr13:26384598..26387742hg19UCSC Ensembl
Outerchr13:25282598..25285742hg18UCSC Ensembl
Outerchr13:25282598..25285742hg17UCSC Ensembl
Cytoband13q12.13
Allele length
AssemblyAllele length
hg386731
hg196731
hg186731
hg176731
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv967
Supporting Variants
SamplesNA18956
Known GenesATP8A2
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)nssv9984
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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