A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5851605



Internal ID22626540
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:76721483..76724435hg38UCSC Ensembl
chr12:77115263..77118215hg19UCSC Ensembl
Cytoband12q21.2
Allele length
AssemblyAllele length
hg382953
hg192953
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17456503, nssv17454997
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5851605
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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