A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17501544



Internal ID22559482
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:12388356..12392937hg38UCSC Ensembl
chr6:12388588..12393169hg19UCSC Ensembl
Cytoband6p24.1
Allele length
AssemblyAllele length
hg384582
hg194582
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5844344
Supporting Variants
Samples
Known GenesRNU6-48P
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17501544
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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