A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv624338



Internal ID15822911
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:38576170..38639618hg38UCSC Ensembl
Outerchr10:38869301..38932749hg19UCSC Ensembl
Outerchr10:38909307..38972755hg18UCSC Ensembl
Outerchr10:38909307..38972755hg17UCSC Ensembl
Cytoband10p11.1
Allele length
AssemblyAllele length
hg3863449
hg1963449
hg1863449
hg1763449
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv510989
Supporting Variants
SamplesNA18994
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)nssv624338
Frequency
Sample Size4
Observed Gain0
Observed Loss0
Observed Complex1
Frequencyn/a


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