A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892964



Internal ID19183784
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:15526909..15689448hg38UCSC Ensembl
Outerchr17:15526909..15689448hg38UCSC Ensembl
Innerchr17:15430223..15592762hg19UCSC Ensembl
Outerchr17:15430223..15592762hg19UCSC Ensembl
Innerchr17:15370948..15533487hg18UCSC Ensembl
Outerchr17:15370948..15533487hg18UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg38162540
hg19162540
hg18162540
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25788017, essv25788189
Samples
Known GenesCDRT1, TRIM16, TVP23C, TVP23C-CDRT4
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892964
Frequency
Sample Size3017
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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