A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17165009



Internal ID21493025
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:102785483..102785483hg38UCSC Ensembl
chrX:102040411..102040411hg19UCSC Ensembl
CytobandXq22.1
Allele length
AssemblyAllele length
hg38131
hg19131
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5604707
Supporting Variants
SamplesNA19238
Known GenesLINC00630
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17165009
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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