A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6985393



Internal ID12971945
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:55894322..55978974hg38UCSC Ensembl
Innerchr10:57654082..57738734hg19UCSC Ensembl
Innerchr10:57324088..57408740hg18UCSC Ensembl
Innerchr10:57324088..57408740hg17UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg3884653
hg1984653
hg1884653
hg1784653
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2750965
Supporting Variants
SamplesBEC_131
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6985393
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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