A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5604169



Internal ID21552836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:56795656..56795706hg38UCSC Ensembl
chr19:57307024..57307074hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17106383
SamplesHG00512
Known GenesZIM2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5604169
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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