A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv7257



Internal ID15536607
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:60711473..60756405hg38UCSC Ensembl
Outerchr16:60745377..60790309hg19UCSC Ensembl
Outerchr16:59302878..59347810hg18UCSC Ensembl
Outerchr16:59302878..59347810hg17UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3844933
hg1944933
hg1844933
hg1744933
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1823
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)nssv7257
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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