A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6420883



Internal ID21078436
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:140321857..140376743hg38UCSC Ensembl
chr7:140021657..140076543hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg3854887
hg1954887
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18217229
Samples
Known GenesSLC37A3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6420883
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