A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18218894



Internal ID20785934
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:102721201..102786600hg38UCSC Ensembl
chr7:102361648..102427047hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg3865400
hg1965400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6606743
Supporting Variants
Samples
Known GenesFAM185A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18218894
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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