A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18223872



Internal ID20790912
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:6840401..7020700hg38UCSC Ensembl
chr7:6880032..7060331hg19UCSC Ensembl
Cytoband7p22.1
Allele length
AssemblyAllele length
hg38180300
hg19180300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6617108
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18223872
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00023


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