A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6990411



Internal ID12980779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:160874284..161011307hg38UCSC Ensembl
Innerchr4:161795436..161932459hg19UCSC Ensembl
Innerchr4:162014886..162151909hg18UCSC Ensembl
Innerchr4:162153041..162290064hg17UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg38137024
hg19137024
hg18137024
hg17137024
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34806
Supporting Variants
SamplesNA18633
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6990411
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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