A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18103489



Internal ID20670529
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:57075127..57075733hg38UCSC Ensembl
chr3:57109155..57109761hg19UCSC Ensembl
Cytoband3p14.3
Allele length
AssemblyAllele length
hg38607
hg19607
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6371329
Supporting Variants
Samples
Known GenesARHGEF3, SPATA12
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18103489
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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