A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5873068



Internal ID22648011
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:43175502..43176501hg38UCSC Ensembl
chr17:41327519..41328518hg19UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg381000
hg191000
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17473827
Samples
Known GenesNBR1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5873068
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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