A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18108064



Internal ID20675104
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:139732145..139734623hg38UCSC Ensembl
chr4:140653299..140655777hg19UCSC Ensembl
Cytoband4q31.1
Allele length
AssemblyAllele length
hg382479
hg192479
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6375818
Supporting Variants
Samples
Known GenesMAML3, MGST2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18108064
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