A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25785381



Internal ID19177142
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:19042022..19143350hg38UCSC Ensembl
Innerchr17:18945335..19046663hg19UCSC Ensembl
Innerchr17:18886060..18987388hg18UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg38101329
hg19101329
hg18101329
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892975
Supporting Variants
Samples
Known GenesGRAP, GRAPL
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=15
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25785381
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