A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4755881



Internal ID20531741
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:68448974..68448974hg38UCSC Ensembl
chr10:70208731..70208731hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg38128
hg19128
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16265653
Samples
Known GenesDNA2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4755881
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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