A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv510580



Internal ID15826604
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:23340137..23400733hg38UCSC Ensembl
Outerchr9:23340135..23400731hg19UCSC Ensembl
Outerchr9:23330135..23390731hg18UCSC Ensembl
Outerchr9:23330135..23390731hg17UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3860597
hg1960597
hg1860597
hg1760597
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv618602
SamplesCHM
Known Genes
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)nsv510580
Frequency
Sample Size4
Observed Gain0
Observed Loss0
Observed Complex1
Frequencyn/a


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