A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17420285



Internal ID22478155
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:56573699..56587555hg38UCSC Ensembl
chr3:56607727..56621583hg19UCSC Ensembl
Cytoband3p14.3
Allele length
AssemblyAllele length
hg3813857
hg1913857
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5899310
Supporting Variants
Samples
Known GenesCCDC66
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17420285
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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