A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5610074



Internal ID21558379
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:100917674..100917674hg38UCSC Ensembl
chrX:100172663..100172663hg19UCSC Ensembl
CytobandXq22.1
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17164854
SamplesHG03371
Known GenesXKRX
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5610074
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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