A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6524895



Internal ID20898256
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:30757355..30760694hg38UCSC Ensembl
chr19:31248262..31251601hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg383340
hg193340
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18047551
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6524895
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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