A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6029236



Internal ID21938579
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:8436894..8443393hg38UCSC Ensembl
chr17:8340212..8346711hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg386500
hg196500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17623712
Samples
Known GenesNDEL1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6029236
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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