A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17394591



Internal ID22452461
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:58648334..58648597hg38UCSC Ensembl
chr20:57223390..57223653hg19UCSC Ensembl
Cytoband20q13.32
Allele length
AssemblyAllele length
hg38264
hg19264
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5961309
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17394591
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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