A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17507950



Internal ID22565899
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:7145611..7146619hg38UCSC Ensembl
chr6:7145844..7146852hg19UCSC Ensembl
Cytoband6p24.3
Allele length
AssemblyAllele length
hg381009
hg191009
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5845362
Supporting Variants
Samples
Known GenesRREB1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17507950
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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