A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5972122



Internal ID22747057
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:39979376..39987701hg38UCSC Ensembl
chrX:39838630..39846955hg19UCSC Ensembl
CytobandXp11.4
Allele length
AssemblyAllele length
hg388326
hg198326
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17516226
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5972122
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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