A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5865778



Internal ID22640713
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:56877927..56883353hg38UCSC Ensembl
chr12:57271711..57277137hg19UCSC Ensembl
Cytoband12q13.3
Allele length
AssemblyAllele length
hg385427
hg195427
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17467542
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5865778
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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