A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18157025



Internal ID20724065
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 StatusS
Merged Variantsnsv6610604
Supporting Variants
Samples
Known GenesGNA12
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18157025
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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