A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4731888



Internal ID20507809
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:12862811..12863103hg38UCSC Ensembl
chr17:12766128..12766420hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg38293
hg19293
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16262071
Samples
Known GenesARHGAP44
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4731888
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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