A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18232144



Internal ID20799184
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:2334546..2335646hg38UCSC Ensembl
chr7:2374181..2375281hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg381101
hg191101
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6619661
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18232144
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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