A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18110471



Internal ID20677511
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:127683826..127684283hg38UCSC Ensembl
chr4:128604981..128605438hg19UCSC Ensembl
Cytoband4q28.1
Allele length
AssemblyAllele length
hg38458
hg19458
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6393332
Supporting Variants
Samples
Known GenesINTU
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18110471
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00045


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