A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17508040



Internal ID22565989
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:78616153..78618872hg38UCSC Ensembl
chr6:79325870..79328589hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg382720
hg192720
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5845452
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17508040
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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