A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6989365



Internal ID12976271
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:108390286..108437062hg38UCSC Ensembl
Innerchr10:110150044..110196820hg19UCSC Ensembl
Innerchr10:110140034..110186810hg18UCSC Ensembl
Innerchr10:110140034..110186810hg17UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg3846777
hg1946777
hg1846777
hg1746777
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2750850
Supporting Variants
SamplesBEC_652
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6989365
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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