A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18223730



Internal ID20790770
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:90183301..90258000hg38UCSC Ensembl
chr7:89812615..89887314hg19UCSC Ensembl
Cytoband7q21.13
Allele length
AssemblyAllele length
hg3874700
hg1974700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6606527
Supporting Variants
Samples
Known GenesC7orf63, STEAP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18223730
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.0002


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