A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6606191



Internal ID20979262
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:116697301..116699700hg38UCSC Ensembl
chr6:117018464..117020863hg19UCSC Ensembl
Cytoband6q22.1
Allele length
AssemblyAllele length
hg382400
hg192400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6374n223
Supporting Variantsnssv18137168
Samples
Known GenesKPNA5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6606191
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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