A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5671838



Internal ID21620146
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:9730207..9730376hg38UCSC Ensembl
chrX:9698247..9698416hg19UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg38170
hg19170
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17169121
SamplesHG00731
Known GenesGPR143
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5671838
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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