A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5971646



Internal ID22746581
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:129740288..129748750hg38UCSC Ensembl
chrX:128874264..128882726hg19UCSC Ensembl
CytobandXq26.1
Allele length
AssemblyAllele length
hg388463
hg198463
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17515345
Samples
Known GenesXPNPEP2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5971646
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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