A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18227592



Internal ID20794632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:43582201..43584200hg38UCSC Ensembl
chr7:43621800..43623799hg19UCSC Ensembl
Cytoband7p13
Allele length
AssemblyAllele length
hg382000
hg192000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6619243
Supporting Variants
Samples
Known GenesSTK17A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18227592
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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