A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17167982



Internal ID21492486
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:45041123..45041426hg38UCSC Ensembl
chrX:44900368..44900671hg19UCSC Ensembl
CytobandXp11.3
Allele length
AssemblyAllele length
hg38304
hg19304
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5667993
Supporting Variants
SamplesNA19238
Known GenesKDM6A
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17167982
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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