A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5978729



Internal ID22753664
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:23507183..23526180hg38UCSC Ensembl
chrX:23525300..23544297hg19UCSC Ensembl
CytobandXp22.11
Allele length
AssemblyAllele length
hg3818998
hg1918998
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17515989
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5978729
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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