A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6987737



Internal ID12634757
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:45573674..45582609hg38UCSC Ensembl
Innerchr17:43651040..43659975hg19UCSC Ensembl
Innerchr17:41006823..41015758hg18UCSC Ensembl
Innerchr17:41006823..41015758hg17UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg388936
hg198936
hg188936
hg178936
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34266
Supporting Variants
SamplesNA18969
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6987737
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