A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5846999



Internal ID22621934
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:45130581..45134929hg38UCSC Ensembl
chr7:45170180..45174528hg19UCSC Ensembl
Cytoband7p13
Allele length
AssemblyAllele length
hg384349
hg194349
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17507056
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5846999
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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