A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6355666



Internal ID21013219
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:97900601..97902400hg38UCSC Ensembl
chr3:97619445..97621244hg19UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg381800
hg191800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18104259
Samples
Known GenesCRYBG3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6355666
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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