A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6987318



Internal ID12631875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:14896187..15806518hg38UCSC Ensembl
Innerchr8:14753696..15664027hg19UCSC Ensembl
Innerchr8:14798067..15708398hg18UCSC Ensembl
Innerchr8:14798067..15708398hg17UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg38910332
hg19910332
hg18910332
hg17910332
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34616
Supporting Variants
SamplesNA10863
Known GenesSGCZ, TUSC3
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6987318
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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