A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6988513



Internal ID12626787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:46089134..46278268hg38UCSC Ensembl
Innerchr17:44166500..44355634hg19UCSC Ensembl
Innerchr17:41522318..41711411hg18UCSC Ensembl
Innerchr17:41522318..41711411hg17UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg38189135
hg19189135
hg18189094
hg17189094
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2751695
Supporting Variants
SamplesBEC_41
Known GenesKANSL1, KANSL1-AS1, LOC644172
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6988513
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