A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1004951



Internal ID19094168
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:10722139..10769464hg38UCSC Ensembl
Innerchr4:10723763..10771088hg19UCSC Ensembl
Innerchr4:10332861..10380186hg18UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg3847326
hg1947326
hg1847326
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3619746
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1004951
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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