A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6433722



Internal ID21091275
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:1593601..1735000hg38UCSC Ensembl
chr8:1541767..1683166hg19UCSC Ensembl
Cytoband8p23.3
Allele length
AssemblyAllele length
hg38141400
hg19141400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18168016
Samples
Known GenesDLGAP2, LOC100507435
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6433722
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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