A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18135605



Internal ID20702646
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:95552244..95555671hg38UCSC Ensembl
chr5:94887948..94891375hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg383428
hg193428
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6398549
Supporting Variants
Samples
Known GenesARSK, TTC37
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18135605
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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