A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18105281



Internal ID20672321
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:81728101..81734400hg38UCSC Ensembl
chr3:81777252..81783551hg19UCSC Ensembl
Cytoband3p12.2
Allele length
AssemblyAllele length
hg386300
hg196300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6375042
Supporting Variants
Samples
Known GenesGBE1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18105281
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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