A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18236714



Internal ID20803754
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:107256092..107323321hg38UCSC Ensembl
chr7:106896537..106963766hg19UCSC Ensembl
Cytoband7q22.3
Allele length
AssemblyAllele length
hg3867230
hg1967230
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6603367
Supporting Variants
Samples
Known GenesCOG5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18236714
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00018


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