A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5972614



Internal ID22747549
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:146956580..146960179hg38UCSC Ensembl
chrX:146038098..146041697hg19UCSC Ensembl
CytobandXq27.3
Allele length
AssemblyAllele length
hg383600
hg193600
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17515595
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5972614
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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