A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6979728



Internal ID12633964
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:42620759..42834322hg38UCSC Ensembl
Innerchr10:43116207..43329770hg19UCSC Ensembl
Innerchr10:42436213..42649776hg18UCSC Ensembl
Innerchr10:42436213..42649776hg17UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg38213564
hg19213564
hg18213564
hg17213564
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 Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6979728
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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