A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5847299



Internal ID22622234
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:6458797..6462096hg38UCSC Ensembl
chr7:6498428..6501727hg19UCSC Ensembl
Cytoband7p22.1
Allele length
AssemblyAllele length
hg383300
hg193300
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17501416
Samples
Known GenesKDELR2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5847299
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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