A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5885009



Internal ID22659993
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:56619240..56660960hg38UCSC Ensembl
chr16:56653152..56694872hg19UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg3841721
hg1941721
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17479013
Samples
Known GenesMT1A, MT1B, MT1DP, MT1E, MT1F, MT1JP, MT1M
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5885009
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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