A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5960287



Internal ID22735272
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:47089406..47089406hg38UCSC Ensembl
chrX:46948805..46948805hg19UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg38341
hg19341
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17465145
Samples
Known GenesRGN
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5960287
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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