A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17434862



Internal ID22492732
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:25359032..25376485hg38UCSC Ensembl
chr7:25398651..25416104hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg3817454
hg1917454
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5920934
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17434862
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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