A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv510193



Internal ID15477691
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:76622129..76628129hg38UCSC Ensembl
Outerchr9:79237045..79243045hg19UCSC Ensembl
Outerchr9:78426865..78432865hg18UCSC Ensembl
Outerchr9:76466599..76472599hg17UCSC Ensembl
Cytoband9q21.13
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 Variantsnssv622177, nssv624081, nssv621357, nssv618314
SamplesCHM, NA15510, NA18994, NA10860
Known GenesPRUNE2
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)nsv510193
Frequency
Sample Size4
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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