A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18119798



Internal ID20686838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:81054180..81080403hg38UCSC Ensembl
chr4:81975334..82001557hg19UCSC Ensembl
Cytoband4q21.21
Allele length
AssemblyAllele length
hg3826224
hg1926224
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6376102
Supporting Variants
Samples
Known GenesBMP3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18119798
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