A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5613736



Internal ID21562041
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:21847579..21847579hg38UCSC Ensembl
chrX:21865697..21865697hg19UCSC Ensembl
CytobandXp22.12
Allele length
AssemblyAllele length
hg38337
hg19337
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17166209
SamplesHG00732
Known GenesMBTPS2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5613736
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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