A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18113396



Internal ID20680436
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:2518105..2525281hg38UCSC Ensembl
chr4:2519832..2527008hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg387177
hg197177
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6374718
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18113396
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