A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5583697



Internal ID21532225
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:35191032..35191368hg38UCSC Ensembl
chr5:35191134..35191470hg19UCSC Ensembl
Cytoband5p13.2
Allele length
AssemblyAllele length
hg38337
hg19337
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17137186
SamplesHG00731
Known GenesPRLR
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5583697
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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