A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5846626



Internal ID22621561
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:45885731..45888305hg38UCSC Ensembl
chr7:45925330..45927904hg19UCSC Ensembl
Cytoband7p12.3
Allele length
AssemblyAllele length
hg382575
hg192575
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17507073
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5846626
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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