A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891672



Internal ID19186068
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:61168587..61206201hg38UCSC Ensembl
Innerchr9:43614545..43654118hg19UCSC Ensembl
Outerchr9:43592096..43675867hg19UCSC Ensembl
Innerchr9:43554541..43594114hg18UCSC Ensembl
Outerchr9:43532092..43615863hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg3837615
hg1983772
hg1883772
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25783433, essv25789479
Samples
Known GenesSPATA31A6
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891672
Frequency
Sample Size3017
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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