A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5607502



Internal ID21555807
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:165708137..165708137hg38UCSC Ensembl
chr1:165677374..165677374hg19UCSC Ensembl
Cytoband1q24.1
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17061055
SamplesHG00732
Known GenesLOC440700
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5607502
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