A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6515989



Internal ID20889350
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:872240..882426hg38UCSC Ensembl
chr19:872240..882426hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3810187
hg1910187
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18050075
Samples
Known GenesMED16
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6515989
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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