A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17445369



Internal ID22503239
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:24080836..24086043hg38UCSC Ensembl
chr7:24120455..24125662hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg385208
hg195208
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5917310
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17445369
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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