A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv510888



Internal ID15826911
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:15170610..15285429hg38UCSC Ensembl
Outerchr4:15172234..15287053hg19UCSC Ensembl
Outerchr4:14781332..14896151hg18UCSC Ensembl
Outerchr4:14848503..14963322hg17UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg38114820
hg19114820
hg18114820
hg17114820
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv621570
SamplesNA15510
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)nsv510888
Frequency
Sample Size4
Observed Gain0
Observed Loss0
Observed Complex1
Frequencyn/a


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