A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155955



Internal ID22086460
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:26392633..26397852hg38UCSC Ensembl
Outerchr3:26384700..26404482hg38UCSC Ensembl
Innerchr3:26434124..26439343hg19UCSC Ensembl
Outerchr3:26426191..26445973hg19UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg3819783
hg1919783
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4016335, nssv4016333, nssv4016332
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155955
Frequency
Sample Size131
Observed Gain1
Observed Loss2
Observed Complex0
Frequencyn/a


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