A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17503677



Internal ID22561618
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:17287266..17289165hg38UCSC Ensembl
chr6:17287497..17289396hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg381900
hg191900
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5844543
Supporting Variants
Samples
Known GenesRBM24
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17503677
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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