A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18123711



Internal ID20690751
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:126177154..126185024hg38UCSC Ensembl
chr5:125512847..125520717hg19UCSC Ensembl
Cytoband5q23.2
Allele length
AssemblyAllele length
hg387871
hg197871
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6401330
Supporting Variants
Samples
Known GenesLOC102546228
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18123711
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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