A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17501649



Internal ID22559588
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:149492315..149507072hg38UCSC Ensembl
chr6:149813451..149828208hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg3814758
hg1914758
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5844079
Supporting Variants
Samples
Known GenesPPIL4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17501649
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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