A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6985630



Internal ID12972469
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:57351455..57492925hg38UCSC Ensembl
Innerchr15:57643653..57785123hg19UCSC Ensembl
Innerchr15:55430945..55572415hg18UCSC Ensembl
Innerchr15:55430945..55572415hg17UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg38141471
hg19141471
hg18141471
hg17141471
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)essv6985630
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