A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5918116



Internal ID22693337
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:66392547..66395203hg38UCSC Ensembl
chr7:65857534..65860190hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg382657
hg192657
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1896n209
Supporting Variantsnssv17434471
Samples
Known GenesLINC00174
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5918116
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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