A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5974941



Internal ID22749876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:103882245..103895041hg38UCSC Ensembl
chrX:103137149..103149962hg19UCSC Ensembl
CytobandXq22.2
Allele length
AssemblyAllele length
hg3812797
hg1912814
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17515056
Samples
Known GenesMIR1256
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5974941
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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