A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18217338



Internal ID20784378
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:73811531..73818000hg38UCSC Ensembl
chr7:73225861..73232330hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg386470
hg196470
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6613991
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18217338
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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