A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6987655



Internal ID12983376
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:176817612..176965646hg38UCSC Ensembl
Innerchr3:176535400..176683434hg19UCSC Ensembl
Innerchr3:178018094..178166128hg18UCSC Ensembl
Innerchr3:178018102..178166136hg17UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg38148035
hg19148035
hg18148035
hg17148035
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2751983
Supporting Variants
SamplesSPC_167
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6987655
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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