A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6607484



Internal ID20980555
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:24627118..24639814hg38UCSC Ensembl
chr7:24666737..24679433hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg3812697
hg1912697
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18155022
Samples
Known GenesMPP6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6607484
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer