A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18100560



Internal ID20667600
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:189646701..189653100hg38UCSC Ensembl
chr3:189364490..189370889hg19UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg386400
hg196400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6363914
Supporting Variants
Samples
Known GenesTP63
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18100560
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.07001


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