A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5669104



Internal ID21617409
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:45040270..45040868hg38UCSC Ensembl
chrX:44899515..44900113hg19UCSC Ensembl
CytobandXp11.3
Allele length
AssemblyAllele length
hg38599
hg19599
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17167978
SamplesNA20847
Known GenesKDM6A
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5669104
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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