A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5847425



Internal ID22622360
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:864435..868440hg38UCSC Ensembl
chr7:904072..908077hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg384006
hg194006
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17503575, nssv17503574
Samples
Known GenesSUN1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5847425
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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