A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6617062



Internal ID20990133
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:147997374..148002590hg38UCSC Ensembl
chr6:148318510..148323726hg19UCSC Ensembl
Cytoband6q24.3
Allele length
AssemblyAllele length
hg385217
hg195217
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18141205
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6617062
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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