A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6356582



Internal ID21014135
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:103523078..103523210hg38UCSC Ensembl
chr3:103241922..103242054hg19UCSC Ensembl
Cytoband3q13.11
Allele length
AssemblyAllele length
hg38133
hg19133
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18091294
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6356582
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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