A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5976558



Internal ID22751493
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:131605432..131635249hg38UCSC Ensembl
chrX:130739430..130769251hg19UCSC Ensembl
CytobandXq26.2
Allele length
AssemblyAllele length
hg3829818
hg1929822
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17515368
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5976558
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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