A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5879735



Internal ID22654707
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:16723544..16752436hg38UCSC Ensembl
chr17:16626858..16655750hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg3828893
hg1928893
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17475525
Samples
Known GenesCCDC144A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5879735
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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