A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18154878



Internal ID20721918
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:22976285..22976823hg38UCSC Ensembl
chr7:23015904..23016442hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg38539
hg19539
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6607599
Supporting Variants
Samples
Known GenesFAM126A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18154878
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00058


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