A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6529695



Internal ID20903056
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:8331134..8361558hg38UCSC Ensembl
chr19:8396018..8426442hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3830425
hg1930425
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18049444
Samples
Known GenesKANK3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6529695
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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