A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5607714



Internal ID21556019
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:63801314..63801314hg38UCSC Ensembl
chrX:63021194..63021194hg19UCSC Ensembl
CytobandXq11.2
Allele length
AssemblyAllele length
hg38358
hg19358
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17168205
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5607714
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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