A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6984693



Internal ID12983346
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:121662406..121760406hg38UCSC Ensembl
Innerchr5:120998101..121096101hg19UCSC Ensembl
Innerchr5:121026000..121124000hg18UCSC Ensembl
Innerchr5:121026000..121124000hg17UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg3898001
hg1998001
hg1898001
hg1798001
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2752059
Supporting Variants
SamplesSPC_166
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6984693
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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