A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4755770



Internal ID20531630
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:31859360..31859360hg38UCSC Ensembl
chr17:30186379..30186379hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16284074
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4755770
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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