A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891727



Internal ID19186123
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:127764326..127819444hg38UCSC Ensembl
Outerchr9:127764326..127819444hg38UCSC Ensembl
Innerchr9:130526605..130581723hg19UCSC Ensembl
Outerchr9:130526605..130581723hg19UCSC Ensembl
Innerchr9:129566426..129621544hg18UCSC Ensembl
Outerchr9:129566426..129621544hg18UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg3855119
hg1955119
hg1855119
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25789026
Samples
Known GenesCDK9, ENG, FPGS, MIR2861, MIR3960, SH2D3C
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891727
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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