A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5845876



Internal ID22620811
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:12474688..12516528hg38UCSC Ensembl
chr7:12514314..12556154hg19UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg3841841
hg1941841
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17509619
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5845876
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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