A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17167659



Internal ID21457400
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:53235874..53235874hg38UCSC Ensembl
chrX:53265056..53265056hg19UCSC Ensembl
CytobandXp11.22
Allele length
AssemblyAllele length
hg381498
hg191498
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5612561
Supporting Variants
SamplesHG02587
Known GenesIQSEC2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17167659
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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