A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17168161



Internal ID21403974
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 StatusS
Merged Variantsnsv5668571
Supporting Variants
SamplesHG00512
Known GenesKIF4A
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17168161
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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