A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1014729



Internal ID19103946
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:121885073..121927811hg38UCSC Ensembl
Innerchr4:122806228..122848966hg19UCSC Ensembl
Innerchr4:123025678..123068416hg18UCSC Ensembl
Cytoband4q27
Allele length
AssemblyAllele length
hg3842739
hg1942739
hg1842739
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3639398
Samples
Known GenesTRPC3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1014729
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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