A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4761507



Internal ID20537367
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:76062508..76062508hg38UCSC Ensembl
chr17:74058589..74058589hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg38137
hg19137
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16266003
Samples
Known GenesSRP68
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4761507
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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