A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5623356



Internal ID21571661
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:151917320..151917320hg38UCSC Ensembl
chrX:151085792..151085792hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg38675
hg19675
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17166101
SamplesHG00731
Known GenesMAGEA4
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5623356
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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