A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5849519



Internal ID22624454
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:38319537..38321272hg38UCSC Ensembl
chr12:38713339..38715074hg19UCSC Ensembl
Cytoband12q12
Allele length
AssemblyAllele length
hg381736
hg191736
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17461980
Samples
Known GenesALG10B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5849519
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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