A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18231506



Internal ID20798546
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:66098098..66135739hg38UCSC Ensembl
chr7:65563085..65600726hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg3837642
hg1937642
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6612881
Supporting Variants
Samples
Known GenesCRCP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18231506
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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