A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18236194



Internal ID20803234
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:73870661..73877707hg38UCSC Ensembl
chr7:73284991..73292037hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg387047
hg197047
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6605201
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18236194
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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