A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6521941



Internal ID20895302
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:12739797..12743199hg38UCSC Ensembl
chr19:12850611..12854013hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg383403
hg193403
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18045372
Samples
Known GenesASNA1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6521941
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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