A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5602433



Internal ID21551091
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:37698149..37699470hg38UCSC Ensembl
chr19:38189050..38190371hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg381322
hg191322
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17104789
SamplesNA18534
Known GenesZNF607
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5602433
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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