A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5868356



Internal ID22643291
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:39788168..39789167hg38UCSC Ensembl
chr17:37944421..37945420hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg381000
hg191000
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17478234
Samples
Known GenesIKZF3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5868356
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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