A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25800961



Internal ID19174344
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:36102943..36139251hg38UCSC Ensembl
Innerchr17:34430336..34466631hg19UCSC Ensembl
Innerchr17:31454449..31490744hg18UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3836309
hg1936296
hg1836296
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893002
Supporting Variants
Samples
Known GenesCCL4
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=11
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25800961
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