A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6403719



Internal ID21061272
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:93067336..93073300hg38UCSC Ensembl
chr6:93777054..93783018hg19UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg385965
hg195965
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18148825
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6403719
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer