A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6982210



Internal ID12626687
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:46099737..46286690hg38UCSC Ensembl
Innerchr17:44177103..44364056hg19UCSC Ensembl
Innerchr17:41532916..41719833hg18UCSC Ensembl
Innerchr17:41532916..41719833hg17UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg38186954
hg19186954
hg18186918
hg17186918
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2751745
Supporting Variants
SamplesBEC_402
Known GenesKANSL1, KANSL1-AS1, LOC644172
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6982210
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