A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17431596



Internal ID22489466
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:83712193..83758075hg38UCSC Ensembl
chr7:83341509..83387391hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg3845883
hg1945883
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5925566
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17431596
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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