A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv7201



Internal ID15536663
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:76569811..76614670hg38UCSC Ensembl
Outerchr15:76862152..76907011hg19UCSC Ensembl
Outerchr15:74649207..74694066hg18UCSC Ensembl
Outerchr15:74649207..74694066hg17UCSC Ensembl
Cytoband15q24.3
Allele length
AssemblyAllele length
hg3844860
hg1944860
hg1844860
hg1744860
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1620
Supporting Variants
SamplesNA12156
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)nssv7201
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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