A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2100



Internal ID15541383
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:22727512..22808665hg38UCSC Ensembl
Outerchr15:23064403..23145589hg19UCSC Ensembl
Outerchr15:20615844..20697030hg18UCSC Ensembl
Outerchr15:20615844..20697030hg17UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3881154
hg1981187
hg1881187
hg1781187
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1460
Supporting Variants
SamplesNA18555
Known GenesLOC283683, NIPA1
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)nssv2100
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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