A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5976871



Internal ID22751806
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:13710857..13712856hg38UCSC Ensembl
chrX:13728976..13730975hg19UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg382000
hg192000
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17515481
Samples
Known GenesTRAPPC2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5976871
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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