A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6602610



Internal ID20975681
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:23599534..23600802hg38UCSC Ensembl
chr7:23639153..23640421hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg381269
hg191269
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18154934
Samples
Known GenesCCDC126
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6602610
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