A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891677



Internal ID18839387
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:68431371..68730207hg38UCSC Ensembl
Outerchr9:68431371..68730207hg38UCSC Ensembl
Innerchr9:71046287..71345123hg19UCSC Ensembl
Outerchr9:71046287..71345123hg19UCSC Ensembl
Innerchr9:70236107..70534943hg18UCSC Ensembl
Outerchr9:70236107..70534943hg18UCSC Ensembl
Cytoband9q13
Allele length
AssemblyAllele length
hg38298837
hg19298837
hg18298837
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25792619
Samples
Known GenesLOC101927015, PGM5, PIP5K1B, TMEM252
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891677
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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