A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25782691



Internal ID19161695
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:76322042..76340464hg38UCSC Ensembl
Innerchr17:74318123..74336545hg19UCSC Ensembl
Innerchr17:71829718..71848140hg18UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg3818423
hg1918423
hg1818423
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893045
Supporting Variants
Samples
Known GenesPRPSAP1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=5
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25782691
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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