A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892969



Internal ID19183789
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:15741192..15768630hg38UCSC Ensembl
Outerchr17:15731113..15768630hg38UCSC Ensembl
Innerchr17:15644506..15671944hg19UCSC Ensembl
Outerchr17:15634427..15671944hg19UCSC Ensembl
Innerchr17:15585231..15612669hg18UCSC Ensembl
Outerchr17:15575152..15612669hg18UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg3837518
hg1937518
hg1837518
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25781244, essv25784248, essv25783509, essv25787257, essv25781893, essv25781449, essv25800688
Samples
Known GenesCDRT15P2, TBC1D26
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892969
Frequency
Sample Size3017
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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