A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5669902



Internal ID21618207
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:137439009..137440319hg38UCSC Ensembl
chrX:136521168..136522478hg19UCSC Ensembl
CytobandXq26.3
Allele length
AssemblyAllele length
hg381311
hg191311
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17165733
SamplesHG03683
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5669902
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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