A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv621612



Internal ID15820960
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:70708447..70732906hg38UCSC Ensembl
Outerchr9:73323363..73347822hg19UCSC Ensembl
Outerchr9:72513183..72537642hg18UCSC Ensembl
Outerchr9:70552917..70577376hg17UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg3824460
hg1924460
hg1824460
hg1724460
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv510944
Supporting Variants
SamplesNA15510
Known GenesTRPM3
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)nssv621612
Frequency
Sample Size4
Observed Gain0
Observed Loss0
Observed Complex1
Frequencyn/a


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