A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5847173



Internal ID22622108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:871491..880118hg38UCSC Ensembl
chr7:911128..919755hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg388628
hg198628
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17503590, nssv17503591
Samples
Known GenesGET4, SUN1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5847173
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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