A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6373315



Internal ID21030868
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:120231497..120248691hg38UCSC Ensembl
chr3:119950344..119967538hg19UCSC Ensembl
Cytoband3q13.33
Allele length
AssemblyAllele length
hg3817195
hg1917195
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18207922
Samples
Known GenesGPR156
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6373315
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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