A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6615357



Internal ID20988428
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:125515185..126154298hg38UCSC Ensembl
chr7:125155239..125794352hg19UCSC Ensembl
Cytoband7q31.33
Allele length
AssemblyAllele length
hg38639114
hg19639114
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18219184
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6615357
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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