A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5919579



Internal ID22694801
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:38957394..38957569hg38UCSC Ensembl
chr7:38996994..38997169hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg38176
hg19176
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17447261
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5919579
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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