A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5631950



Internal ID21580255
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:97260908..97260908hg38UCSC Ensembl
chr6:97708784..97708784hg19UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg38300
hg19300
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17150846
SamplesHG00731
Known GenesMIR548H3, MMS22L
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5631950
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