A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5665922



Internal ID21614227
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:70373648..70373717hg38UCSC Ensembl
chrX:69593498..69593567hg19UCSC Ensembl
CytobandXq13.1
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17168162
SamplesHG00731
Known GenesKIF4A
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5665922
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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