A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6516444



Internal ID20889805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:15026619..15062297hg38UCSC Ensembl
chr19:15137431..15173108hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg3835679
hg1935678
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18044396
Samples
Known GenesCASP14
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6516444
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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