A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17062614



Internal ID21487797
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:208551379..208565378hg38UCSC Ensembl
chr1:208724724..208738723hg19UCSC Ensembl
Cytoband1q32.2
Allele length
AssemblyAllele length
hg3814000
hg1914000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5582512
Supporting Variants
SamplesNA18534
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17062614
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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