A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18135326



Internal ID20702366
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:105614533..105616506hg38UCSC Ensembl
chr6:106062408..106064381hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg381974
hg191974
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6607222
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18135326
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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