A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5597521



Internal ID21546136
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:35045650..35045718hg38UCSC Ensembl
chr19:35536554..35536622hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17104490
SamplesHG00731
Known GenesHPN
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5597521
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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