A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6522519



Internal ID20895880
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:2897399..2901693hg38UCSC Ensembl
chr19:2897397..2901691hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg384295
hg194295
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18047433
Samples
Known GenesZNF57
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6522519
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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