A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6982892



Internal ID12975711
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:125454172..125684437hg38UCSC Ensembl
Innerchr2:126211749..126442014hg19UCSC Ensembl
Innerchr2:125928219..126158484hg18UCSC Ensembl
Innerchr2:125927979..126158244hg17UCSC Ensembl
Cytoband2q14.3
Allele length
AssemblyAllele length
hg38230266
hg19230266
hg18230266
hg17230266
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2751825
Supporting Variants
SamplesBEC_608
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6982892
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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