A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5916992



Internal ID22692211
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:66543779..66550948hg38UCSC Ensembl
chr7:66008766..66015935hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg387170
hg197170
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17436527
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5916992
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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