A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18221722



Internal ID20788762
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:90363545..91393930hg38UCSC Ensembl
chr7:89992859..91023245hg19UCSC Ensembl
Cytoband7q21.13
Allele length
AssemblyAllele length
hg381030386
hg191030387
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6619367
Supporting Variants
Samples
Known GenesCDK14, CLDN12, FZD1, GTPBP10, LOC101409256
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18221722
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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