A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5921052



Internal ID22696275
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:29151774..29152930hg38UCSC Ensembl
chr7:29191390..29192546hg19UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg381157
hg191157
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17437310
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5921052
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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