A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6535101



Internal ID20908462
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:8327557..8332691hg38UCSC Ensembl
chr19:8392441..8397575hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg385135
hg195135
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18049442
Samples
Known GenesKANK3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6535101
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