A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6529200



Internal ID20902561
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:41155970..41177865hg38UCSC Ensembl
chr19:41661875..41683770hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3821896
hg1921896
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18048062
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6529200
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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