A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5951772



Internal ID22676447
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:75234624..75234624hg38UCSC Ensembl
chrX:74454459..74454459hg19UCSC Ensembl
CytobandXq13.3
Allele length
AssemblyAllele length
hg38275
hg19275
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17454968
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5951772
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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