A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6431613



Internal ID21089166
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:52115113..52115858hg38UCSC Ensembl
chr8:53027673..53028418hg19UCSC Ensembl
Cytoband8q11.23
Allele length
AssemblyAllele length
hg38746
hg19746
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18168290
Samples
Known GenesST18
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6431613
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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