A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6600915



Internal ID20973986
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:12181401..12183200hg38UCSC Ensembl
chr7:12221027..12222826hg19UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg381800
hg191800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18225887
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6600915
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