A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1919



Internal ID15199796
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:87963774..87979608hg38UCSC Ensembl
Outerchr16:87997380..88013214hg19UCSC Ensembl
Outerchr16:86554881..86570715hg18UCSC Ensembl
Outerchr16:86554881..86570715hg17UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg3815835
hg1915835
hg1815835
hg1715835
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv6690
SamplesNA12156
Known GenesBANP
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)nsv1919
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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