A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17472312



Internal ID22530204
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:75435411..75441675hg38UCSC Ensembl
chr15:75727752..75734016hg19UCSC Ensembl
Cytoband15q24.2
Allele length
AssemblyAllele length
hg386265
hg196265
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5855013
Supporting Variants
Samples
Known GenesSIN3A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17472312
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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