A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18093320



Internal ID20660360
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:108570324..108575330hg38UCSC Ensembl
chr3:108289171..108294177hg19UCSC Ensembl
Cytoband3q13.13
Allele length
AssemblyAllele length
hg385007
hg195007
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6363729
Supporting Variants
Samples
Known GenesKIAA1524
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18093320
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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