A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892957



Internal ID19183777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:8710144..8729992hg38UCSC Ensembl
Outerchr17:8710144..8729992hg38UCSC Ensembl
Innerchr17:8613462..8633310hg19UCSC Ensembl
Outerchr17:8613462..8633310hg19UCSC Ensembl
Innerchr17:8554187..8574035hg18UCSC Ensembl
Outerchr17:8554187..8574035hg18UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg3819849
hg1919849
hg1819849
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25779475
Samples
Known GenesCCDC42
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892957
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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