A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5604707



Internal ID21523109
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 StatusM
Merged Variants
Supporting Variantsnssv17165009
SamplesNA19238
Known GenesLINC00630
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5604707
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer