A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9311



Internal ID15540262
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:20469355..20514279hg38UCSC Ensembl
Outerchr16:20480677..20525601hg19UCSC Ensembl
Outerchr16:20388178..20433102hg18UCSC Ensembl
Outerchr16:20388178..20433102hg17UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg3844925
hg1944925
hg1844925
hg1744925
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7279
Supporting Variants
SamplesNA18517
Known GenesACSM2A
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)nssv9311
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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