A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5975283



Internal ID22750218
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:75560813..75566868hg38UCSC Ensembl
chrX:74780648..74786703hg19UCSC Ensembl
CytobandXq13.3
Allele length
AssemblyAllele length
hg386056
hg196056
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2284n209
Supporting Variantsnssv17516735
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5975283
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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