A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5916670



Internal ID22691889
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:149035272..149046505hg38UCSC Ensembl
chr7:148732364..148743597hg19UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg3811234
hg1911234
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17440910
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5916670
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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