A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1265



Internal ID15544459
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:76573323..76611953hg38UCSC Ensembl
Outerchr15:76865664..76904294hg19UCSC Ensembl
Outerchr15:74652719..74691349hg18UCSC Ensembl
Outerchr15:74652719..74691349hg17UCSC Ensembl
Cytoband15q24.3
Allele length
AssemblyAllele length
hg3838631
hg1938631
hg1838631
hg1738631
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1620
Supporting Variants
SamplesNA19240
Known GenesSCAPER
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)nssv1265
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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