A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6603802



Internal ID20976873
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:122747432..122751591hg38UCSC Ensembl
chr6:123068577..123072736hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg384160
hg194160
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18137405
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6603802
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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