A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892996



Internal ID19183816
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:34065327..34072955hg38UCSC Ensembl
Outerchr17:34065327..34072955hg38UCSC Ensembl
Innerchr17:32392346..32399974hg19UCSC Ensembl
Outerchr17:32392346..32399974hg19UCSC Ensembl
Innerchr17:29416459..29424087hg18UCSC Ensembl
Outerchr17:29416459..29424087hg18UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg387629
hg197629
hg187629
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25782483, essv25784543
Samples
Known GenesASIC2
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892996
Frequency
Sample Size3017
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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