A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5973323



Internal ID22748258
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:56447954..56478575hg38UCSC Ensembl
chrX:56474387..56505008hg19UCSC Ensembl
CytobandXp11.21
Allele length
AssemblyAllele length
hg3830622
hg1930622
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17516404, nssv17516405
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5973323
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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