A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6034121



Internal ID21943464
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:76073300..76073588hg38UCSC Ensembl
chr17:74069381..74069669hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg38289
hg19289
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17630377
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6034121
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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