A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5852258



Internal ID22627193
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:155225987..155227329hg38UCSC Ensembl
chr7:155017697..155019039hg19UCSC Ensembl
Cytoband7q36.2
Allele length
AssemblyAllele length
hg381343
hg191343
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17504641
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5852258
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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