A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18228130



Internal ID20795170
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:16644188..16731149hg38UCSC Ensembl
chr7:16683813..16770774hg19UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg3886962
hg1986962
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6607011
Supporting Variants
Samples
Known GenesANKMY2, BZW2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18228130
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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