A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4201



Internal ID15538928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:20465853..20518015hg38UCSC Ensembl
Outerchr16:20477175..20529337hg19UCSC Ensembl
Outerchr16:20384676..20436838hg18UCSC Ensembl
Outerchr16:20384676..20436838hg17UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg3852163
hg1952163
hg1852163
hg1752163
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7279
Supporting Variants
SamplesNA12878
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)nssv4201
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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