A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6526149



Internal ID20899510
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:51402178..51402361hg38UCSC Ensembl
chr19:51905432..51905615hg19UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg38184
hg19184
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18048715
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6526149
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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