A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5979777



Internal ID22754712
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:68542193..68553305hg38UCSC Ensembl
chrX:67762035..67773147hg19UCSC Ensembl
CytobandXq12
Allele length
AssemblyAllele length
hg3811113
hg1911113
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17516664
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5979777
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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