A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156026



Internal ID22086531
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:151247995..151252914hg38UCSC Ensembl
Outerchr3:151235890..151255577hg38UCSC Ensembl
Innerchr3:150965783..150970702hg19UCSC Ensembl
Outerchr3:150953678..150973365hg19UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg3819688
hg1919688
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4015923, nssv4015921, nssv4015920, nssv4015922
Samples
Known GenesMED12L, P2RY14
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156026
Frequency
Sample Size131
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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