A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5975766



Internal ID22750701
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:86004769..86010089hg38UCSC Ensembl
chrX:85259773..85265093hg19UCSC Ensembl
CytobandXq21.2
Allele length
AssemblyAllele length
hg385321
hg195321
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17516877
Samples
Known GenesCHM
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5975766
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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