A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6988849



Internal ID12983521
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:162145671..162238888hg38UCSC Ensembl
Innerchr3:161863459..161956676hg19UCSC Ensembl
Innerchr3:163346153..163439370hg18UCSC Ensembl
Innerchr3:163346161..163439378hg17UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg3893218
hg1993218
hg1893218
hg1793218
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2751981
Supporting Variants
SamplesSPC_18
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6988849
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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