A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv510955



Internal ID15826977
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:19440418..19525520hg38UCSC Ensembl
Outerchr7:19480041..19565143hg19UCSC Ensembl
Outerchr7:19446566..19531668hg18UCSC Ensembl
Outerchr7:19253281..19338383hg17UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg3885103
hg1985103
hg1885103
hg1785103
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv624313, nssv621596
SamplesNA15510, NA18994
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)nsv510955
Frequency
Sample Size4
Observed Gain0
Observed Loss0
Observed Complex2
Frequencyn/a


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