A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6525237



Internal ID20898598
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:9325021..9325521hg38UCSC Ensembl
chr19:9435697..9436197hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38501
hg19501
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18050131
Samples
Known GenesZNF559, ZNF559-ZNF177
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6525237
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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