A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6982960



Internal ID12627901
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:106744610..106932839hg38UCSC Ensembl
Innerchr4:107665767..107853996hg19UCSC Ensembl
Innerchr4:107885216..108073445hg18UCSC Ensembl
Innerchr4:108023371..108211600hg17UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg38188230
hg19188230
hg18188230
hg17188230
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2752020
Supporting Variants
SamplesBEC_529
Known GenesDKK2
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6982960
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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