A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5976900



Internal ID22751835
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:71736118..71736118hg38UCSC Ensembl
chr16:71770021..71770021hg19UCSC Ensembl
Cytoband16q22.2
Allele length
AssemblyAllele length
hg38196
hg19196
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17375123
Samples
Known GenesAP1G1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5976900
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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