A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1136



Internal ID15199013
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:96240437..96285541hg38UCSC Ensembl
Outerchr13:96892691..96937795hg19UCSC Ensembl
Outerchr13:95690692..95735796hg18UCSC Ensembl
Outerchr13:95690692..95735796hg17UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg3845105
hg1945105
hg1845105
hg1745105
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv9151
SamplesNA12156
Known GenesHS6ST3
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)nsv1136
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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