A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18102865



Internal ID20669905
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:56948811..56952275hg38UCSC Ensembl
chr3:56982839..56986303hg19UCSC Ensembl
Cytoband3p14.3
Allele length
AssemblyAllele length
hg383465
hg193465
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6355971
Supporting Variants
Samples
Known GenesARHGEF3, ARHGEF3-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18102865
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00316


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