A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18233180



Internal ID20800220
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:23665501..23729800hg38UCSC Ensembl
chr7:23705120..23769419hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg3864300
hg1964300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6601337
Supporting Variants
Samples
Known GenesFAM221A, STK31
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18233180
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00076


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