A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2151



Internal ID15541434
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:76020966..76049688hg38UCSC Ensembl
Outerchr16:76054864..76083586hg19UCSC Ensembl
Outerchr16:74612365..74641087hg18UCSC Ensembl
Outerchr16:74612365..74641087hg17UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg387132
hg197132
hg187132
hg177132
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv1882
Supporting Variants
SamplesNA18555
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)nssv2151
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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