A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6986337



Internal ID12628058
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:100658517..100709093hg38UCSC Ensembl
Innerchr3:100377361..100427937hg19UCSC Ensembl
Innerchr3:101860051..101910627hg18UCSC Ensembl
Innerchr3:101860051..101910627hg17UCSC Ensembl
Cytoband3q12.2
Allele length
AssemblyAllele length
hg3850577
hg1950577
hg1850577
hg1750577
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2751968
Supporting Variants
SamplesBEC_537
Known GenesGPR128
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6986337
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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