A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6517390



Internal ID20890751
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:52495165..52538330hg38UCSC Ensembl
chr19:52998418..53041583hg19UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg3843166
hg1943166
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3697n223
Supporting Variantsnssv18048794
Samples
Known GenesZNF578, ZNF808
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6517390
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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