A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17449212



Internal ID22507082
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:137849076..137849727hg38UCSC Ensembl
chr7:137533822..137534473hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg38652
hg19652
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5918801
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17449212
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001


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