A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17501096



Internal ID22559033
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:117294649..117302937hg38UCSC Ensembl
chr6:117615812..117624100hg19UCSC Ensembl
Cytoband6q22.1
Allele length
AssemblyAllele length
hg388289
hg198289
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5844326
Supporting Variants
Samples
Known GenesROS1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17501096
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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