A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6401687



Internal ID21059240
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:95591623..95592194hg38UCSC Ensembl
chr5:94927327..94927898hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg38572
hg19572
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18135608
Samples
Known GenesARSK
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6401687
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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