A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6527077



Internal ID20900438
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:35453728..35456538hg38UCSC Ensembl
chr19:35944630..35947440hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg382811
hg192811
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18046287
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6527077
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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