A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10064



Internal ID15542733
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:74533883..74563554hg38UCSC Ensembl
Outerchr15:74826224..74855895hg19UCSC Ensembl
Outerchr15:72613277..72642948hg18UCSC Ensembl
Outerchr15:72613277..72642948hg17UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg388490
hg198490
hg188490
hg178490
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv1611
Supporting Variants
SamplesNA18956
Known GenesARID3B
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)nssv10064
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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