A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18231261



Internal ID20798301
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:136416501..136420100hg38UCSC Ensembl
chr7:136101249..136104848hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg383600
hg193600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6424967
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18231261
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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