A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892417



Internal ID19183237
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:88474880..88591667hg38UCSC Ensembl
Outerchr13:88474880..88591667hg38UCSC Ensembl
Innerchr13:89127135..89243922hg19UCSC Ensembl
Outerchr13:89127135..89243922hg19UCSC Ensembl
Innerchr13:87925136..88041923hg18UCSC Ensembl
Outerchr13:87925136..88041923hg18UCSC Ensembl
Cytoband13q31.2
Allele length
AssemblyAllele length
hg38116788
hg19116788
hg18116788
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25787186
Samples
Known GenesLINC00433
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892417
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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