A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5896367



Internal ID22671459
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:56572234..56582133hg38UCSC Ensembl
chr3:56606262..56616161hg19UCSC Ensembl
Cytoband3p14.3
Allele length
AssemblyAllele length
hg389900
hg199900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17411943
Samples
Known GenesCCDC66
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5896367
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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