A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5195n100



Internal ID19015563
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:40676645..40785736hg38UCSC Ensembl
chr4:40678662..40787753hg19UCSC Ensembl
chr4:40373419..40482510hg18UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg38109092
hg19109092
hg18109092
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1006924, nsv1013466, nsv1007860, nsv1011844, nsv1007528, nsv999107
Samples
Known GenesNSUN7
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv5195n100
Frequency
Sample Size29084
Observed Gain11
Observed Loss0
Observed Complex0
Frequencyn/a


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