A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25783433



Internal ID19166061
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:61168587..61228370hg38UCSC Ensembl
Innerchr9:43592096..43654118hg19UCSC Ensembl
Innerchr9:43532092..43594114hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg3859784
hg1962023
hg1862023
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891672
Supporting Variants
Samples
Known GenesSPATA31A6
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=5
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25783433
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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