A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5846824



Internal ID22621759
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:32594529..32622759hg38UCSC Ensembl
chr7:32634141..32662371hg19UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg3828231
hg1928231
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17505512
Samples
Known GenesDPY19L1P1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5846824
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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