A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5970972



Internal ID22745907
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:63375006..63408005hg38UCSC Ensembl
chrX:62594885..62627885hg19UCSC Ensembl
CytobandXq11.1
Allele length
AssemblyAllele length
hg3833000
hg1933001
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17516527
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5970972
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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