A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5883756



Internal ID22658738
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:16315746..16321290hg38UCSC Ensembl
chr17:16219060..16224604hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg385545
hg195545
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17475508
Samples
Known GenesPIGL
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5883756
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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