A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6609651



Internal ID20982722
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:124922501..124924100hg38UCSC Ensembl
chr7:124562555..124564154hg19UCSC Ensembl
Cytoband7q31.33
Allele length
AssemblyAllele length
hg381600
hg191600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18150226
Samples
Known GenesPOT1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6609651
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