A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5843268



Internal ID22618203
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:88672693..88673918hg38UCSC Ensembl
chr5:87968511..87969736hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg381226
hg191226
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17499511, nssv17499510
Samples
Known GenesLINC00461
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5843268
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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