A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6026658



Internal ID21936001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:76020047..76020106hg38UCSC Ensembl
chr17:74016128..74016187hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17633541
Samples
Known GenesEVPL
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6026658
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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