A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5854893



Internal ID22629828
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:74395353..74396673hg38UCSC Ensembl
chr7:73809683..73811003hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg381321
hg191321
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17502780, nssv17502779
Samples
Known GenesCLIP2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5854893
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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