A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6989256



Internal ID12972513
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:10191807..10207627hg38UCSC Ensembl
Innerchr4:10193431..10209251hg19UCSC Ensembl
Innerchr4:9802529..9818349hg18UCSC Ensembl
Innerchr4:9869700..9885520hg17UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg3815821
hg1915821
hg1815821
hg1715821
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)essv6989256
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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