A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv510988



Internal ID15478482
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:26878769..27008111hg38UCSC Ensembl
Outerchr10:27167698..27297040hg19UCSC Ensembl
Outerchr10:27207704..27337046hg18UCSC Ensembl
Outerchr10:27207704..27337046hg17UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg38129343
hg19129343
hg18129343
hg17129343
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv618610
SamplesCHM
Known GenesANKRD26, LINC00202-1
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)nsv510988
Frequency
Sample Size4
Observed Gain0
Observed Loss0
Observed Complex1
Frequencyn/a


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