A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5607497



Internal ID21555802
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:149490732..149490732hg38UCSC Ensembl
chrX:148572263..148572263hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg38176
hg19176
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17165911
SamplesNA19983
Known GenesIDS
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5607497
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