A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18159832



Internal ID20726872
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:90727393..90740382hg38UCSC Ensembl
chr7:90356707..90369697hg19UCSC Ensembl
Cytoband7q21.13
Allele length
AssemblyAllele length
hg3812990
hg1912991
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6612840
Supporting Variants
Samples
Known GenesCDK14
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18159832
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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