A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17165662



Internal ID21475285
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:129343260..129343373hg38UCSC Ensembl
chrX:128477237..128477350hg19UCSC Ensembl
CytobandXq25
Allele length
AssemblyAllele length
hg38114
hg19114
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5665601
Supporting Variants
SamplesHG03371
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17165662
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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