A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17506512



Internal ID22564460
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:53990767..53994631hg38UCSC Ensembl
chr6:53855565..53859429hg19UCSC Ensembl
Cytoband6p12.1
Allele length
AssemblyAllele length
hg383865
hg193865
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5845649
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17506512
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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