A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6406516



Internal ID21064069
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:94572490..94585032hg38UCSC Ensembl
chr5:93908195..93920737hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg3812543
hg1912543
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18136467
Samples
Known GenesKIAA0825
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6406516
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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