A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18120280



Internal ID20687320
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:76754401..76755300hg38UCSC Ensembl
chr4:77675554..77676453hg19UCSC Ensembl
Cytoband4q21.1
Allele length
AssemblyAllele length
hg38900
hg19900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6383261
Supporting Variants
Samples
Known GenesSHROOM3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18120280
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00026


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