A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6519095



Internal ID20892456
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:2691496..2693296hg38UCSC Ensembl
chr19:2691494..2693294hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg381801
hg191801
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18046067
Samples
Known GenesGNG7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6519095
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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