A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv618928



Internal ID15472046
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:76361018..76415969hg38UCSC Ensembl
Outerchr15:76653359..76708310hg19UCSC Ensembl
Outerchr15:74440414..74495365hg18UCSC Ensembl
Outerchr15:74440414..74495365hg17UCSC Ensembl
Cytoband15q24.3
Allele length
AssemblyAllele length
hg3854952
hg1954952
hg1854952
hg1754952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv510667
Supporting Variants
SamplesNA10860
Known GenesSCAPER
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)nssv618928
Frequency
Sample Size4
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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