A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5669008



Internal ID21617313
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:19811183..19813084hg38UCSC Ensembl
chrX:19829301..19831202hg19UCSC Ensembl
CytobandXp22.12
Allele length
AssemblyAllele length
hg381902
hg191902
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17166185
SamplesHG02587
Known GenesSH3KBP1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5669008
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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