A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156028



Internal ID22086533
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:152629305..152638413hg38UCSC Ensembl
Outerchr3:152625038..152638694hg38UCSC Ensembl
Innerchr3:152347094..152356202hg19UCSC Ensembl
Outerchr3:152342827..152356483hg19UCSC Ensembl
Cytoband3q25.2
Allele length
AssemblyAllele length
hg3813657
hg1913657
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4015926, nssv4015925
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156028
Frequency
Sample Size131
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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