A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892973



Internal ID18837107
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:15952882..16027568hg38UCSC Ensembl
Outerchr17:15947882..16030711hg38UCSC Ensembl
Innerchr17:15856196..15930882hg19UCSC Ensembl
Outerchr17:15851196..15934025hg19UCSC Ensembl
Innerchr17:15796921..15871607hg18UCSC Ensembl
Outerchr17:15791921..15874750hg18UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg3882830
hg1982830
hg1882830
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25791244, essv25793052, essv25788232, essv25790596, essv25790268
Samples
Known GenesADORA2B, NCOR1, TTC19, ZSWIM7
MethodSNP array
Analysis
PlatformIllumina HumanHap 550
Illumina HumanHap 610
Illumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892973
Frequency
Sample Size3017
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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