A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5608532



Internal ID21556837
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:37876520..37876520hg38UCSC Ensembl
chrX:37735773..37735773hg19UCSC Ensembl
CytobandXp11.4
Allele length
AssemblyAllele length
hg38134
hg19134
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17167344
SamplesHG03486
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5608532
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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