A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18025294



Internal ID20592334
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:57657731..57658207hg38UCSC Ensembl
chr15:57949929..57950405hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg38477
hg19477
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6504464
Supporting Variants
Samples
Known GenesGCOM1, MYZAP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18025294
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00026


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