A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6405529



Internal ID21063082
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:94338240..94578121hg38UCSC Ensembl
chr5:93673945..93913826hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg38239882
hg19239882
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18136451
Samples
Known GenesKIAA0825
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6405529
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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