A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5635990



Internal ID21584295
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:96805012..96805012hg38UCSC Ensembl
chr5:96140715..96140715hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg38318
hg19318
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17152153
SamplesHG03125
Known GenesERAP1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5635990
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