A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5870733



Internal ID22645669
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:49011527..49012897hg38UCSC Ensembl
chr17:47088889..47090259hg19UCSC Ensembl
Cytoband17q21.32
Allele length
AssemblyAllele length
hg381371
hg191371
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17474517
Samples
Known GenesIGF2BP1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5870733
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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