A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6984566



Internal ID12977212
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:45094335..45294489hg38UCSC Ensembl
Innerchr10:45589783..45789937hg19UCSC Ensembl
Innerchr10:44909789..45109943hg18UCSC Ensembl
Innerchr10:44909789..45109943hg17UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg38200155
hg19200155
hg18200155
hg17200155
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2750897
Supporting Variants
SamplesBEC_720
Known GenesANKRD30BP3, MIR3156-1, RSU1P2
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6984566
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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