A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019205



Internal ID18761739
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:147603701..147655114hg38UCSC Ensembl
Innerchr4:148524852..148576265hg19UCSC Ensembl
Innerchr4:148744302..148795715hg18UCSC Ensembl
Cytoband4q31.23
Allele length
AssemblyAllele length
hg3851414
hg1951414
hg1851414
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3636066
Samples
Known GenesPRMT10, TMEM184C
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1019205
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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