A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6983782



Internal ID12629239
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:101312253..101663253hg38UCSC Ensembl
Innerchr10:103072010..103423010hg19UCSC Ensembl
Innerchr10:103062000..103413000hg18UCSC Ensembl
Innerchr10:103062000..103413000hg17UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg38351001
hg19351001
hg18351001
hg17351001
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2750847
Supporting Variants
SamplesBEC_626
Known GenesBTRC, DPCD, FBXW4, MIR3158-1, MIR3158-2, POLL
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6983782
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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