A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25779177



Internal ID19174605
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:15093691..15144382hg38UCSC Ensembl
Innerchr17:14997008..15047699hg19UCSC Ensembl
Innerchr17:14937733..14988424hg18UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg3850692
hg1950692
hg1850692
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892963
Supporting Variants
Samples
Known GenesCDRT8
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=14
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25779177
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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