A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6979727



Internal ID12633965
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:42620746..42799146hg38UCSC Ensembl
Innerchr10:43116194..43294594hg19UCSC Ensembl
Innerchr10:42436200..42614600hg18UCSC Ensembl
Innerchr10:42436200..42614600hg17UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg38178401
hg19178401
hg18178401
hg17178401
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34929
Supporting Variants
SamplesNA18620
Known GenesBMS1, ZNF33B
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6979727
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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