A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2933



Internal ID15541620
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:51549695..51583579hg38UCSC Ensembl
Outerchr15:51841892..51875776hg19UCSC Ensembl
Outerchr15:49629184..49663068hg18UCSC Ensembl
Outerchr15:49629184..49663068hg17UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg385752
hg195752
hg185752
hg175752
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1535
Supporting Variants
SamplesNA18555
Known GenesDMXL2
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)nssv2933
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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