A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1008332



Internal ID18750863
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:12269..62089hg38UCSC Ensembl
Innerchr4:12269..61981hg19UCSC Ensembl
Innerchr4:2269..51981hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3849821
hg1949713
hg1849713
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5054n100
Supporting Variantsnssv3619374
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)nsv1008332
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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