A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25787186



Internal ID19173725
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:88474880..88591667hg38UCSC Ensembl
Innerchr13:89127135..89243922hg19UCSC Ensembl
Innerchr13:87925136..88041923hg18UCSC Ensembl
Cytoband13q31.2
Allele length
AssemblyAllele length
hg38116788
hg19116788
hg18116788
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892417
Supporting Variants
Samples
Known GenesLINC00433
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=34
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25787186
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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