A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5855835



Internal ID22630770
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:51084736..51088435hg38UCSC Ensembl
chr12:51478519..51482218hg19UCSC Ensembl
Cytoband12q13.12
Allele length
AssemblyAllele length
hg383700
hg193700
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17457596
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5855835
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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