A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25796194



Internal ID18816768
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:39162812..39172813hg38UCSC Ensembl
Innerchr17:37319065..37329066hg19UCSC Ensembl
Innerchr17:34572591..34582592hg18UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3810002
hg1910002
hg1810002
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893011
Supporting Variants
Samples
Known GenesARL5C
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=5
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25796194
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer