A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25779649



Internal ID19172385
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:13384528..13486624hg38UCSC Ensembl
Innerchr17:13287845..13389941hg19UCSC Ensembl
Innerchr17:13228570..13330666hg18UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg38102097
hg19102097
hg18102097
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892960
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=27
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25779649
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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