A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6395943



Internal ID21053496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:83629224..83631283hg38UCSC Ensembl
chr6:84338943..84341002hg19UCSC Ensembl
Cytoband6q14.2
Allele length
AssemblyAllele length
hg382060
hg192060
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18145913
Samples
Known GenesSNAP91
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6395943
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