A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5613748



Internal ID21562053
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:151743041..151743041hg38UCSC Ensembl
chrX:150911513..150911513hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17166098, nssv17166099
SamplesHG00731, HG01596
Known GenesCNGA2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5613748
Frequency
Sample Size35
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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