A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6668



Internal ID15537195
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:32142513..32823798hg38UCSC Ensembl
Outerchr16:32153834..32835119hg19UCSC Ensembl
Outerchr16:32061335..32742620hg18UCSC Ensembl
Outerchr16:32061335..32742620hg17UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg38681286
hg19681286
hg18681286
hg17681286
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7281
Supporting Variants
SamplesNA12156
Known GenesHERC2P4, LOC390705, TP53TG3, TP53TG3B, TP53TG3C, TP53TG3D
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)nssv6668
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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