A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5895005



Internal ID22670082
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:102715969..102716317hg38UCSC Ensembl
chr3:102434813..102435161hg19UCSC Ensembl
Cytoband3q12.3
Allele length
AssemblyAllele length
hg38349
hg19349
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17409427
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5895005
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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