A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6606889



Internal ID20979960
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:110072601..110096600hg38UCSC Ensembl
chr6:110393804..110417803hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3824000
hg1924000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6362n223
Supporting Variantsnssv18136659
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6606889
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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