A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv623208



Internal ID15821781
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:26091038..26097038hg38UCSC Ensembl
Outerchr16:26102359..26108359hg19UCSC Ensembl
Outerchr16:26009860..26015860hg18UCSC Ensembl
Outerchr16:26009860..26015860hg17UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg386001
hg196001
hg186001
hg176001
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv507811
Supporting Variants
SamplesNA18994
Known GenesHS3ST4
MethodOptical mapping
AnalysisSingle-molecule optical maps were assembled into genome-wide consensus maps. These consensus maps were compared to a restriction map generated from the NCBI b35 human genome reference sequence.
PlatformOptical Mapping
Comments
ReferenceTeague_et_al_2010
Pubmed ID20534489
Accession Number(s)nssv623208
Frequency
Sample Size4
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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