A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4753027



Internal ID20528887
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:76377855..76377855hg38UCSC Ensembl
chr17:74373936..74373936hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg38297
hg19297
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16275864
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4753027
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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