A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18032726



Internal ID20599766
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:75572231..75574325hg38UCSC Ensembl
chr16:75606129..75608223hg19UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg382095
hg192095
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6513318
Supporting Variants
Samples
Known GenesGABARAPL2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18032726
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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