A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17473827



Internal ID22531721
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:43175502..43176501hg38UCSC Ensembl
chr17:41327519..41328518hg19UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg381000
hg191000
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5873068
Supporting Variants
Samples
Known GenesNBR1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17473827
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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