A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6397735



Internal ID21055288
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:95560864..95563972hg38UCSC Ensembl
chr5:94896568..94899676hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg383109
hg193109
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18135606
Samples
Known GenesARSK
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6397735
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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