A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5877077



Internal ID22652040
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:53058065..53061000hg38UCSC Ensembl
chr16:53091977..53094912hg19UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg382936
hg192936
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17471590
Samples
Known GenesCHD9
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5877077
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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