A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6989525



Internal ID12973997
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:93610311..93742908hg38UCSC Ensembl
Innerchr15:94153540..94286137hg19UCSC Ensembl
Innerchr15:91954544..92087141hg18UCSC Ensembl
Innerchr15:91954544..92087141hg17UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38132598
hg19132598
hg18132598
hg17132598
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2751543
Supporting Variants
SamplesBEC_492
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6989525
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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