A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17501558



Internal ID22559496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:12613851..12615392hg38UCSC Ensembl
chr6:12614083..12615624hg19UCSC Ensembl
Cytoband6p24.1
Allele length
AssemblyAllele length
hg381542
hg191542
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5844357
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17501558
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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