A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv617380



Internal ID15816535
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:76780782..76842616hg38UCSC Ensembl
Outerchr10:78540540..78602374hg19UCSC Ensembl
Outerchr10:78210546..78272380hg18UCSC Ensembl
Outerchr10:78210546..78272380hg17UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg3861835
hg1961835
hg1861835
hg1761835
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv508595
Supporting Variants
SamplesCHM
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)nssv617380
Frequency
Sample Size4
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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