A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18103511



Internal ID20670551
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:59049601..59050200hg38UCSC Ensembl
chr3:59035327..59035926hg19UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg38600
hg19600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6370963
Supporting Variants
Samples
Known GenesC3orf67
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18103511
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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