A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6986643



Internal ID12632066
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:140290178..140741386hg38UCSC Ensembl
Innerchr3:140009020..140460228hg19UCSC Ensembl
Innerchr3:141491710..141942918hg18UCSC Ensembl
Innerchr3:141491718..141942926hg17UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg38451209
hg19451209
hg18451209
hg17451209
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34489
Supporting Variants
SamplesNA11994
Known GenesCLSTN2, CLSTN2-AS1, TRIM42
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6986643
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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