A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17485952



Internal ID22543865
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:38594914..38602413hg38UCSC Ensembl
chr20:37223557..37231056hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg387500
hg197500
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5876480
Supporting Variants
Samples
Known GenesARHGAP40
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17485952
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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