A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17507263



Internal ID22565211
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:63784709..63787458hg38UCSC Ensembl
chr6:64494602..64497351hg19UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg382750
hg192750
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5845693
Supporting Variants
Samples
Known GenesEYS
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17507263
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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