A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6615380



Internal ID20988451
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:31581831..31583744hg38UCSC Ensembl
chr7:31621445..31623358hg19UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg381914
hg191914
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18219615
Samples
Known GenesCCDC129
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6615380
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