A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6076393



Internal ID21985626
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:155480391..155480391hg38UCSC Ensembl
chr7:155273086..155273086hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg38293
hg19293
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17566999
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6076393
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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