A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6988561



Internal ID12628617
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:187118866..188059749hg38UCSC Ensembl
Innerchr4:188040020..188980903hg19UCSC Ensembl
Innerchr4:188277014..189217897hg18UCSC Ensembl
Innerchr4:188415169..189356052hg17UCSC Ensembl
Cytoband4q35.2
Allele length
AssemblyAllele length
hg38940884
hg19940884
hg18940884
hg17940884
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2752041
Supporting Variants
SamplesBEC_573
Known GenesLOC339975, ZFP42
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6988561
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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