A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5951501



Internal ID22726861
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:47090921..47090921hg38UCSC Ensembl
chrX:46950320..46950320hg19UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17465142
Samples
Known GenesRGN
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5951501
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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