A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18025292



Internal ID20592332
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:57587413..57617917hg38UCSC Ensembl
chr15:57879611..57910115hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg3830505
hg1930505
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6508079
Supporting Variants
Samples
Known GenesGCOM1, MYZAP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18025292
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