A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5884033



Internal ID22659015
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:31370083..31375339hg38UCSC Ensembl
chr17:29697101..29702357hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg385257
hg195257
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17478112
Samples
Known GenesNF1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5884033
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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