A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6029934



Internal ID21939277
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:2964180..2964270hg38UCSC Ensembl
chr17:2867474..2867564hg19UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg3891
hg1991
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17633538
Samples
Known GenesRAP1GAP2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6029934
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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