A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6981407



Internal ID12972065
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:136755501..136842783hg38UCSC Ensembl
Innerchr8:137767744..137855026hg19UCSC Ensembl
Innerchr8:137836926..137924208hg18UCSC Ensembl
Innerchr8:137836926..137924208hg17UCSC Ensembl
Cytoband8q24.23
Allele length
AssemblyAllele length
hg3887283
hg1987283
hg1887283
hg1787283
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2752221
Supporting Variants
SamplesBEC_177
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6981407
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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