A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6530997



Internal ID20904358
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:11046059..11046793hg38UCSC Ensembl
chr19:11156735..11157469hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38735
hg19735
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18044967
Samples
Known GenesSMARCA4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6530997
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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