A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5876715



Internal ID22651676
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:57691466..57696117hg38UCSC Ensembl
chr16:57725378..57730029hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg384652
hg194652
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17479017
Samples
Known GenesCCDC135
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5876715
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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