A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18065588



Internal ID20632628
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:93830730..93837034hg38UCSC Ensembl
chr1:94296286..94302590hg19UCSC Ensembl
Cytoband1p22.1
Allele length
AssemblyAllele length
hg386305
hg196305
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6328052
Supporting Variants
Samples
Known GenesBCAR3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18065588
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00033


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