A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18225444



Internal ID20792484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:29168935..29499002hg38UCSC Ensembl
chr7:29208551..29538618hg19UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg38330068
hg19330068
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6600391
Supporting Variants
Samples
Known GenesCHN2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18225444
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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