A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18219459



Internal ID20786499
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:19223736..19975909hg38UCSC Ensembl
chr7:19263359..20015532hg19UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg38752174
hg19752174
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6604787
Supporting Variants
Samples
Known GenesMIR3146, TMEM196, TWISTNB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18219459
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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