A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6981687



Internal ID12972525
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:10124515..10265454hg38UCSC Ensembl
Innerchr4:10126139..10267078hg19UCSC Ensembl
Innerchr4:9735237..9876176hg18UCSC Ensembl
Innerchr4:9802408..9943347hg17UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg38140940
hg19140940
hg18140940
hg17140940
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2752053
Supporting Variants
SamplesBEC_319
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6981687
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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