A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17167980



Internal ID21410857
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:45040661..45040710hg38UCSC Ensembl
chrX:44899906..44899955hg19UCSC Ensembl
CytobandXp11.3
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5672058
Supporting Variants
SamplesHG00513
Known GenesKDM6A
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17167980
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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