A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1006806



Internal ID18749337
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:29013..94493hg38UCSC Ensembl
Innerchr4:29013..94380hg19UCSC Ensembl
Innerchr4:19013..84380hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3865481
hg1965368
hg1865368
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5063n100
Supporting Variantsnssv3615253
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)nsv1006806
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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