A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156



Internal ID15545719
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:102541399..102586683hg38UCSC Ensembl
Outerchr13:103193749..103239033hg19UCSC Ensembl
Outerchr13:101991750..102037034hg18UCSC Ensembl
Outerchr13:101991750..102037034hg17UCSC Ensembl
Cytoband13q33.1
Allele length
AssemblyAllele length
hg3845285
hg1945285
hg1845285
hg1745285
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv9157
SamplesNA12156
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)nsv1156
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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