A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6530618



Internal ID20903979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:56402996..56403529hg38UCSC Ensembl
chr19:56914365..56914898hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg38534
hg19534
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18049318
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6530618
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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