A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18092151



Internal ID20659191
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:113991084..113994360hg38UCSC Ensembl
chr3:113709931..113713207hg19UCSC Ensembl
Cytoband3q13.31
Allele length
AssemblyAllele length
hg383277
hg193277
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6368145
Supporting Variants
Samples
Known GenesKIAA1407
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18092151
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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