A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25785733



Internal ID19171367
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:900770..917084hg38UCSC Ensembl
Innerchr17:804010..820324hg19UCSC Ensembl
Innerchr17:750760..767074hg18UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg3816315
hg1916315
hg1816315
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892943
Supporting Variants
Samples
Known GenesNXN
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=15
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25785733
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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