A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv510989



Internal ID15827011
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:38576170..38692715hg38UCSC Ensembl
Outerchr10:38869301..38985846hg19UCSC Ensembl
Outerchr10:38909307..39025852hg18UCSC Ensembl
Outerchr10:38909307..39025852hg17UCSC Ensembl
Cytoband10p11.1
Allele length
AssemblyAllele length
hg38116546
hg19116546
hg18116546
hg17116546
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv624338, nssv622400
SamplesNA18994, NA10860
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)nsv510989
Frequency
Sample Size4
Observed Gain0
Observed Loss0
Observed Complex2
Frequencyn/a


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