A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6526943



Internal ID20900304
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:14241272..14245055hg38UCSC Ensembl
chr19:14352084..14355867hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg383784
hg193784
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18045914
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6526943
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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