A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6525602



Internal ID20898963
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:35623993..35627961hg38UCSC Ensembl
chr19:36114895..36118863hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg383969
hg193969
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18046300
Samples
Known GenesHAUS5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6525602
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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