A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17472927



Internal ID22530819
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:56793779..56811137hg38UCSC Ensembl
chr15:57085977..57103335hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg3817359
hg1917359
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5851516
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17472927
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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