A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6989984



Internal ID12977202
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:45054697..45324688hg38UCSC Ensembl
Innerchr10:45550145..45820136hg19UCSC Ensembl
Innerchr10:44870151..45140142hg18UCSC Ensembl
Innerchr10:44870151..45140142hg17UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg38269992
hg19269992
hg18269992
hg17269992
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, OR13A1, RSU1P2
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6989984
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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