A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4015921



Internal ID22077552
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 Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1156026
Supporting Variants
Samples
Known GenesMED12L, P2RY14
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4015921
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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