A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv507495



Internal ID15823525
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:135172307..135178307hg38UCSC Ensembl
Outerchr8:136184550..136190550hg19UCSC Ensembl
Outerchr8:136253732..136259732hg18UCSC Ensembl
Outerchr8:136253732..136259732hg17UCSC Ensembl
Cytoband8q24.22
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 Variantsnssv623060, nssv620437
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)nsv507495
Frequency
Sample Size4
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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