A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5914129



Internal ID22689345
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:43032142..43032277hg38UCSC Ensembl
chr7:43071741..43071876hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg38136
hg19136
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17436526
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5914129
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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