A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5976412



Internal ID22751347
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:64260971..64262940hg38UCSC Ensembl
chrX:63480851..63482820hg19UCSC Ensembl
CytobandXq11.2
Allele length
AssemblyAllele length
hg381970
hg191970
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17516545
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5976412
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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