A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17168805



Internal ID21447109
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:97185423..97185480hg38UCSC Ensembl
chrX:96440422..96440479hg19UCSC Ensembl
CytobandXq21.33
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5668157
Supporting Variants
SamplesHG00732
Known GenesDIAPH2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17168805
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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