A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5611175



Internal ID21559480
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:120581889..120581889hg38UCSC Ensembl
chrX:119715744..119715744hg19UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg38354
hg19354
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17165115
SamplesNA18534
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5611175
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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