A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5980294



Internal ID22755229
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:3735829..3739551hg38UCSC Ensembl
chrX:3653870..3657592hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg383723
hg193723
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17516197
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5980294
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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