A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17167301



Internal ID21430399
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:44552498..44552634hg38UCSC Ensembl
chrX:44411744..44411880hg19UCSC Ensembl
CytobandXp11.3
Allele length
AssemblyAllele length
hg38137
hg19137
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5665322
Supporting Variants
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17167301
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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