A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6990075



Internal ID12978050
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:26219484..26315707hg38UCSC Ensembl
Innerchr14:26688690..26784913hg19UCSC Ensembl
Innerchr14:25758530..25854753hg18UCSC Ensembl
Innerchr14:25758530..25854753hg17UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg3896224
hg1996224
hg1896224
hg1796224
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2751270
Supporting Variants
SamplesBEC_95
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6990075
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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