A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1009127



Internal ID18751658
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:29013..66074hg38UCSC Ensembl
Innerchr4:29013..65966hg19UCSC Ensembl
Innerchr4:19013..55966hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3837062
hg1936954
hg1836954
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5062n100
Supporting Variantsnssv3738059
Samples
Known GenesZNF595, ZNF718
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1009127
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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