A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6981656



Internal ID12972472
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:57366802..57472370hg38UCSC Ensembl
Innerchr15:57659000..57764568hg19UCSC Ensembl
Innerchr15:55446292..55551860hg18UCSC Ensembl
Innerchr15:55446292..55551860hg17UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg38105569
hg19105569
hg18105569
hg17105569
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2751536
Supporting Variants
SamplesBEC_312
Known GenesCGNL1
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6981656
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer