A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5976824



Internal ID22751759
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:21251053..21255932hg38UCSC Ensembl
chrX:21269171..21274050hg19UCSC Ensembl
CytobandXp22.12
Allele length
AssemblyAllele length
hg384880
hg194880
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17515962
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5976824
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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