A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5961172



Internal ID22652360
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:23134573..23134573hg38UCSC Ensembl
chr10:23423502..23423502hg19UCSC Ensembl
Cytoband10p12.2
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17349856
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5961172
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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