A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2751270



Internal ID12984822
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 StatusM
Merged Variants
Supporting Variantsessv6985089, essv6990075, essv6989474
SamplesBEC_95
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
CommentsSample level SV from stringent call set
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)esv2751270
Frequency
Sample Size771
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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