A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5859693



Internal ID22634628
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:156078001..156080137hg38UCSC Ensembl
chr7:155870695..155872831hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg382137
hg192137
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17504645
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5859693
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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