A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv509356



Internal ID15825382
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:69606162..69668319hg38UCSC Ensembl
Outerchr10:71365918..71428075hg19UCSC Ensembl
Outerchr10:71035924..71098081hg18UCSC Ensembl
Outerchr10:71035924..71098081hg17UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg384461
hg194461
hg184461
hg174461
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv621040
SamplesNA15510
Known GenesC10orf35
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)nsv509356
Frequency
Sample Size4
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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