A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6526582



Internal ID20899943
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:37784488..37829771hg38UCSC Ensembl
chr19:38275128..38320411hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg3845284
hg1945284
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18046677
Samples
Known GenesLOC100631378, LOC644554
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6526582
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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