A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5889579



Internal ID22664598
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:7153340..7263545hg38UCSC Ensembl
chr3:7195027..7305232hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38110206
hg19110206
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17414863
Samples
Known GenesGRM7
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5889579
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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