A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6985089



Internal ID12978044
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:26233654..26310154hg38UCSC Ensembl
Innerchr14:26702860..26779360hg19UCSC Ensembl
Innerchr14:25772700..25849200hg18UCSC Ensembl
Innerchr14:25772700..25849200hg17UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg3876501
hg1976501
hg1876501
hg1776501
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)essv6985089
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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