A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5849882



Internal ID22624817
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:61806997..61817000hg38UCSC Ensembl
chr12:62200778..62210781hg19UCSC Ensembl
Cytoband12q14.1
Allele length
AssemblyAllele length
hg3810004
hg1910004
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17459211
Samples
Known GenesFAM19A2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5849882
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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