A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5973858



Internal ID22748793
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:21280966..21296363hg38UCSC Ensembl
chrX:21299084..21314481hg19UCSC Ensembl
CytobandXp22.12
Allele length
AssemblyAllele length
hg3815398
hg1915398
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17515964
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5973858
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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