A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6982961



Internal ID12627883
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:106765008..106958916hg38UCSC Ensembl
Innerchr4:107686165..107880073hg19UCSC Ensembl
Innerchr4:107905614..108099522hg18UCSC Ensembl
Innerchr4:108043769..108237677hg17UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg38193909
hg19193909
hg18193909
hg17193909
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)essv6982961
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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