A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6515728



Internal ID20889089
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:9197650..9200145hg38UCSC Ensembl
chr19:9308326..9310821hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg382496
hg192496
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18050121
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6515728
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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