A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv508605



Internal ID15824632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:105908160..105973075hg38UCSC Ensembl
Outerchr10:107667918..107732833hg19UCSC Ensembl
Outerchr10:107657908..107722823hg18UCSC Ensembl
Outerchr10:107657908..107722823hg17UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg3864916
hg1964916
hg1864916
hg1764916
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv620138
SamplesNA15510
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)nsv508605
Frequency
Sample Size4
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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