A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5929595



Internal ID22704851
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:9577057..9577454hg38UCSC Ensembl
chr20:9557704..9558101hg19UCSC Ensembl
Cytoband20p12.2
Allele length
AssemblyAllele length
hg38398
hg19398
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17402782
Samples
Known GenesPAK7
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5929595
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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