A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1462



Internal ID15546025
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:23739258..23753065hg38UCSC Ensembl
Outerchr15:23984405..23998212hg19UCSC Ensembl
Outerchr15:21535498..21549305hg18UCSC Ensembl
Outerchr15:21535498..21549305hg17UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3813808
hg1913808
hg1813808
hg1713808
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv5540
SamplesNA19129
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)nsv1462
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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