A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18096487



Internal ID20663527
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:156532697..156534024hg38UCSC Ensembl
chr3:156250486..156251813hg19UCSC Ensembl
Cytoband3q25.31
Allele length
AssemblyAllele length
hg381328
hg191328
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6366037
Supporting Variants
Samples
Known GenesKCNAB1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18096487
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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