A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6518604



Internal ID20891965
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:14539101..14542500hg38UCSC Ensembl
chr19:14649913..14653312hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg383400
hg193400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18045946
Samples
Known GenesTECR
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6518604
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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