A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18092632



Internal ID20659672
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:106767511..107170186hg38UCSC Ensembl
chr3:106486358..106889033hg19UCSC Ensembl
Cytoband3q13.12
Allele length
AssemblyAllele length
hg38402676
hg19402676
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6368527
Supporting Variants
Samples
Known GenesLINC00882
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18092632
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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