A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5975601



Internal ID22750536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:76120607..76134106hg38UCSC Ensembl
chrX:75340442..75353941hg19UCSC Ensembl
CytobandXq13.3
Allele length
AssemblyAllele length
hg3813500
hg1913500
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17516745
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5975601
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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