A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18158332



Internal ID20725372
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:7690245..7704002hg38UCSC Ensembl
chr7:7729876..7743633hg19UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg3813758
hg1913758
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6607337
Supporting Variants
Samples
Known GenesRPA3, RPA3-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18158332
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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