A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5605641



Internal ID21553946
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:107910768..107910768hg38UCSC Ensembl
chrX:107153998..107153998hg19UCSC Ensembl
CytobandXq22.3
Allele length
AssemblyAllele length
hg38237
hg19237
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17164881
SamplesHG00731
Known GenesMID2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5605641
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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