A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18139912



Internal ID20706952
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:169180752..170050020hg38UCSC Ensembl
chr6:169580847..170365244hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38869269
hg19784398
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6608026
Supporting Variants
Samples
Known GenesC6orf120, ERMARD, LINC00242, LINC00574, PHF10, TCTE3, THBS2, WDR27
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18139912
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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