A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6035413



Internal ID21944756
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:40753566..40753718hg38UCSC Ensembl
chr17:38909818..38909970hg19UCSC Ensembl
Cytoband17q21.2
Allele length
AssemblyAllele length
hg38153
hg19153
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17630283
Samples
Known GenesKRT25
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6035413
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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