A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6605452



Internal ID20978523
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:122300994..122304499hg38UCSC Ensembl
chr6:122622140..122625644hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg383506
hg193505
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18137361
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6605452
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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