A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5972494



Internal ID22747429
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:88842752..88871089hg38UCSC Ensembl
chrX:88097753..88126090hg19UCSC Ensembl
CytobandXq21.31
Allele length
AssemblyAllele length
hg3828338
hg1928338
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17516911
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5972494
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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