A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5847682



Internal ID22622617
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:3381891..3382890hg38UCSC Ensembl
chr11:3403121..3404120hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg381000
hg191000
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17458587
Samples
Known GenesLOC650368
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5847682
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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