A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5967958



Internal ID22742893
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:64837698..64862791hg38UCSC Ensembl
chrX:64057578..64082671hg19UCSC Ensembl
CytobandXq11.2
Allele length
AssemblyAllele length
hg3825094
hg1925094
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17516605
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5967958
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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