A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9312



Internal ID15540263
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:20501518..20559504hg38UCSC Ensembl
Outerchr16:20512840..20570826hg19UCSC Ensembl
Outerchr16:20420341..20478327hg18UCSC Ensembl
Outerchr16:20420341..20478327hg17UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg3857987
hg1957987
hg1857987
hg1757987
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7279
Supporting Variants
SamplesNA18517
Known GenesACSM2B
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)nssv9312
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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