A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18143034



Internal ID20710074
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:166247687..166248893hg38UCSC Ensembl
chr6:166661175..166662381hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg381207
hg191207
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6614743
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18143034
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00011


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