A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5846443



Internal ID22621378
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:19878413..19891990hg38UCSC Ensembl
chr7:19918036..19931613hg19UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg3813578
hg1913578
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17504709
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5846443
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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