A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6982959



Internal ID12627900
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:106732239..106959239hg38UCSC Ensembl
Innerchr4:107653396..107880396hg19UCSC Ensembl
Innerchr4:107872845..108099845hg18UCSC Ensembl
Innerchr4:108011000..108238000hg17UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg38227001
hg19227001
hg18227001
hg17227001
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 Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6982959
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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