A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25792770



Internal ID19160768
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:77012989..77027306hg38UCSC Ensembl
Innerchr17:75009071..75023388hg19UCSC Ensembl
Innerchr17:72520666..72534983hg18UCSC Ensembl
Cytoband17q25.2
Allele length
AssemblyAllele length
hg3814318
hg1914318
hg1814318
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893046
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=10
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25792770
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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