A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5668571



Internal ID21616876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:70373577..70373718hg38UCSC Ensembl
chrX:69593427..69593568hg19UCSC Ensembl
CytobandXq13.1
Allele length
AssemblyAllele length
hg38142
hg19142
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17168161
SamplesHG00512
Known GenesKIF4A
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5668571
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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