A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5855700



Internal ID22630635
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:57353109..57354908hg38UCSC Ensembl
chr12:57746892..57748691hg19UCSC Ensembl
Cytoband12q13.3
Allele length
AssemblyAllele length
hg381800
hg191800
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv416n209
Supporting Variantsnssv17456066, nssv17454258
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5855700
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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