A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18228078



Internal ID20795118
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:14974501..14996200hg38UCSC Ensembl
chr7:15014126..15035825hg19UCSC Ensembl
Cytoband7p21.2
Allele length
AssemblyAllele length
hg3821700
hg1921700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6620018
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18228078
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00062


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