A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5959291



Internal ID22734327
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:140514503..140514503hg38UCSC Ensembl
chrX:139596668..139596668hg19UCSC Ensembl
CytobandXq27.1
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17440944
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5959291
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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