A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5970695



Internal ID22745630
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:122230037..122237758hg38UCSC Ensembl
chrX:121363890..121371611hg19UCSC Ensembl
CytobandXq25
Allele length
AssemblyAllele length
hg387722
hg197722
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17515282
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5970695
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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