A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6525871



Internal ID20899232
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:36256601..36259000hg38UCSC Ensembl
chr19:36747503..36749902hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg382400
hg192400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18046344
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6525871
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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