A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5920112



Internal ID22695335
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:51650118..51650210hg38UCSC Ensembl
chr7:51717814..51717906hg19UCSC Ensembl
Cytoband7p12.1
Allele length
AssemblyAllele length
hg3893
hg1993
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17433875
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5920112
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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