A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6524641



Internal ID20898002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:33776560..33806449hg38UCSC Ensembl
chr19:34267465..34297354hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg3829890
hg1929890
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18046189
Samples
Known GenesKCTD15
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6524641
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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