A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5838682



Internal ID22613617
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:168977017..168978916hg38UCSC Ensembl
chr4:169898168..169900067hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg381900
hg191900
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17493607
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5838682
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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