A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18224249



Internal ID20791289
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:44142372..44143015hg38UCSC Ensembl
chr7:44181971..44182614hg19UCSC Ensembl
Cytoband7p13
Allele length
AssemblyAllele length
hg38644
hg19644
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6618889
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18224249
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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