A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18225667



Internal ID20792707
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:101526138..101698760hg38UCSC Ensembl
chr7:101169419..101342040hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg38172623
hg19172622
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6610311
Supporting Variants
Samples
Known GenesCOL26A1, LINC01007, MYL10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18225667
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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