A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5959810



Internal ID22734829
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:121167807..121167807hg38UCSC Ensembl
chrX:120301661..120301661hg19UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg38223
hg19223
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17439184
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5959810
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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