A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6615063



Internal ID20988134
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:125750040..125877742hg38UCSC Ensembl
chr7:125390094..125517796hg19UCSC Ensembl
Cytoband7q31.33
Allele length
AssemblyAllele length
hg38127703
hg19127703
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18221552
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6615063
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