A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25786765



Internal ID19178929
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:242355..253678hg38UCSC Ensembl
Innerchr17:92146..103469hg19UCSC Ensembl
Innerchr17:92146..103469hg18UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg3811324
hg1911324
hg1811324
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892942
Supporting Variants
Samples
Known GenesRPH3AL
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=7
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25786765
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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