A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6985998



Internal ID12635816
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:2652868..3037058hg38UCSC Ensembl
Innerchr10:2695060..3079250hg19UCSC Ensembl
Innerchr10:2685060..3069250hg18UCSC Ensembl
Innerchr10:2685060..3069250hg17UCSC Ensembl
Cytoband10p15.2
Allele length
AssemblyAllele length
hg38384191
hg19384191
hg18384191
hg17384191
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34832
Supporting Variants
SamplesNA19201
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6985998
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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