A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv509838



Internal ID15825864
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:87629089..87635089hg38UCSC Ensembl
Outerchr3:87678239..87684239hg19UCSC Ensembl
Outerchr3:87760929..87766929hg18UCSC Ensembl
Outerchr3:87760929..87766929hg17UCSC Ensembl
Cytoband3p11.2
Allele length
AssemblyAllele length
hg386001
hg196001
hg186001
hg176001
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv623913, nssv621559
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)nsv509838
Frequency
Sample Size4
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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