A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv508044



Internal ID15824071
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:169227097..169233097hg38UCSC Ensembl
Outerchr1:169196335..169202335hg19UCSC Ensembl
Outerchr1:167462959..167468959hg18UCSC Ensembl
Outerchr1:165927993..165933993hg17UCSC Ensembl
Cytoband1q24.2
Allele length
AssemblyAllele length
hg386001
hg196001
hg186001
hg176001
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv624222, nssv622298
SamplesNA18994, NA10860
Known GenesNME7
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)nsv508044
Frequency
Sample Size4
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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