A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17165261



Internal ID21471066
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:11610255..11610255hg38UCSC Ensembl
chrX:11628375..11628375hg19UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg38578
hg19578
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5618457
Supporting Variants
SamplesHG03125
Known GenesARHGAP6
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17165261
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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