A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6038920



Internal ID21948263
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:3010156..3015617hg38UCSC Ensembl
chr17:2913450..2918911hg19UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg385462
hg195462
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17630312
Samples
Known GenesRAP1GAP2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6038920
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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