A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv7258



Internal ID15536606
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:62346085..62373063hg38UCSC Ensembl
Outerchr16:62379989..62406967hg19UCSC Ensembl
Outerchr16:60937490..60964468hg18UCSC Ensembl
Outerchr16:60937490..60964468hg17UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3826979
hg1926979
hg1826979
hg1726979
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1825
Supporting Variants
SamplesNA12156
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)nssv7258
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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