A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892958



Internal ID19183778
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:10064697..10082524hg38UCSC Ensembl
Outerchr17:10064697..10082524hg38UCSC Ensembl
Innerchr17:9968014..9985841hg19UCSC Ensembl
Outerchr17:9968014..9985841hg19UCSC Ensembl
Innerchr17:9908739..9926566hg18UCSC Ensembl
Outerchr17:9908739..9926566hg18UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg3817828
hg1917828
hg1817828
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25782693
Samples
Known GenesGAS7
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892958
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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