A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6031713



Internal ID21941056
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:51878841..51878894hg38UCSC Ensembl
chr17:49956201..49956254hg19UCSC Ensembl
Cytoband17q21.33
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17624911
Samples
Known GenesCA10
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6031713
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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