A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10931



Internal ID15539519
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:54916509..54955004hg38UCSC Ensembl
Outerchr15:55208707..55247202hg19UCSC Ensembl
Outerchr15:52995999..53034494hg18UCSC Ensembl
Outerchr15:52995999..53034494hg17UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg3838496
hg1938496
hg1838496
hg1738496
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv1541
Supporting Variants
SamplesNA15510
Known Genes
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)nssv10931
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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