A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5894695



Internal ID22669770
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:177486764..177487059hg38UCSC Ensembl
chr5:176913765..176914060hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg38296
hg19296
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17416346
Samples
Known GenesPDLIM7
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5894695
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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