A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6610604



Internal ID20983675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:2746861..2785876hg38UCSC Ensembl
chr7:2786495..2825510hg19UCSC Ensembl
Cytoband7p22.2
Allele length
AssemblyAllele length
hg3839016
hg1939016
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18157025
Samples
Known GenesGNA12
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6610604
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