A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5610177



Internal ID21558482
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:123408870..123408870hg38UCSC Ensembl
chrX:122542721..122542721hg19UCSC Ensembl
CytobandXq25
Allele length
AssemblyAllele length
hg38522
hg19522
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17165309
SamplesHG00864
Known GenesGRIA3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5610177
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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