A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1013824



Internal ID19103043
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:4292300..4334097hg38UCSC Ensembl
Innerchr4:4294027..4335824hg19UCSC Ensembl
Innerchr4:4344928..4386725hg18UCSC Ensembl
Cytoband4p16.2
Allele length
AssemblyAllele length
hg3841798
hg1941798
hg1841798
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3616172
Samples
Known GenesZBTB49
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1013824
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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