A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5949201



Internal ID22724652
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:90317500..90317500hg38UCSC Ensembl
chr7:89946814..89946814hg19UCSC Ensembl
Cytoband7q21.13
Allele length
AssemblyAllele length
hg38500
hg19500
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17445403
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5949201
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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