A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17165695



Internal ID21445434
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:132610869..132611294hg38UCSC Ensembl
chrX:131744897..131745322hg19UCSC Ensembl
CytobandXq26.2
Allele length
AssemblyAllele length
hg38426
hg19426
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5667480
Supporting Variants
SamplesHG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17165695
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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