A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6039800



Internal ID21949143
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:78201518..78212115hg38UCSC Ensembl
chr17:76197599..76208196hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg3810598
hg1910598
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17625320
Samples
Known GenesAFMID
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6039800
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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