A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6978038



Internal ID12631823
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:104959432..105139432hg38UCSC Ensembl
Innerchr6:105407307..105587307hg19UCSC Ensembl
Innerchr6:105514000..105694000hg18UCSC Ensembl
Innerchr6:105514000..105694000hg17UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg38180001
hg19180001
hg18180001
hg17180001
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34842
Supporting Variants
SamplesNA10859
Known GenesBVES, BVES-AS1, LIN28B
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6978038
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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