A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5975417



Internal ID22750352
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:3964404..3974244hg38UCSC Ensembl
chrX:3882445..3892285hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg389841
hg199841
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17516223
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5975417
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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