A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv7283



Internal ID15536581
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:81548032..81592900hg38UCSC Ensembl
Outerchr16:81581637..81626505hg19UCSC Ensembl
Outerchr16:80139138..80184006hg18UCSC Ensembl
Outerchr16:80139138..80184006hg17UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg3844869
hg1944869
hg1844869
hg1744869
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1898
Supporting Variants
SamplesNA12156
Known GenesCMIP
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)nssv7283
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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