A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv7170



Internal ID15536694
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:51984096..52028722hg38UCSC Ensembl
Outerchr15:52276293..52320919hg19UCSC Ensembl
Outerchr15:50063585..50108211hg18UCSC Ensembl
Outerchr15:50063585..50108211hg17UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg3844627
hg1944627
hg1844627
hg1744627
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1536
Supporting Variants
SamplesNA12156
Known GenesMAPK6
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)nssv7170
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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