A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6526672



Internal ID20900033
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:57070804..57081312hg38UCSC Ensembl
chr19:57582172..57592680hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg3810509
hg1910509
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18048536
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6526672
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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