A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5974427



Internal ID22749362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:131840372..131848883hg38UCSC Ensembl
chrX:130974400..130982911hg19UCSC Ensembl
CytobandXq26.2
Allele length
AssemblyAllele length
hg388512
hg198512
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17515379
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5974427
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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