A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6521589



Internal ID20894950
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:17261817..17266222hg38UCSC Ensembl
chr19:17372626..17377031hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg384406
hg194406
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18045170
Samples
Known GenesUSHBP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6521589
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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