A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17431508



Internal ID22489378
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:56391289..56401635hg38UCSC Ensembl
chr6:56256087..56266433hg19UCSC Ensembl
Cytoband6p12.1
Allele length
AssemblyAllele length
hg3810347
hg1910347
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5905188
Supporting Variants
Samples
Known GenesRNU6-71P
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17431508
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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