A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5840975



Internal ID22615910
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:107669225..107676664hg38UCSC Ensembl
chr5:107004926..107012365hg19UCSC Ensembl
Cytoband5q21.3
Allele length
AssemblyAllele length
hg387440
hg197440
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17492994
Samples
Known GenesEFNA5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5840975
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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