A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6603488



Internal ID20976559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:124896551..124909557hg38UCSC Ensembl
chr7:124536605..124549611hg19UCSC Ensembl
Cytoband7q31.33
Allele length
AssemblyAllele length
hg3813007
hg1913007
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18217429
Samples
Known GenesPOT1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6603488
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