A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6527237



Internal ID20900598
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:17990355..17991092hg38UCSC Ensembl
chr19:18101164..18101901hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg38738
hg19738
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18045056
Samples
Known GenesKCNN1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6527237
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