A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5598150



Internal ID21546772
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:8419709..8420050hg38UCSC Ensembl
chr19:8484593..8484934hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38342
hg19342
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17106734
SamplesHG03065
Known GenesMARCH2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5598150
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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