A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5918159



Internal ID22693380
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:82642201..82642515hg38UCSC Ensembl
chr7:82271517..82271831hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg38315
hg19315
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17429687
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5918159
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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