A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25790829



Internal ID19176524
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:6757307..6990209hg38UCSC Ensembl
Innerchr10:6799269..7032171hg19UCSC Ensembl
Innerchr10:6839275..7072177hg18UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg38232903
hg19232903
hg18232903
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891751
Supporting Variants
Samples
Known GenesLINC00706, LINC00707
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=94
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25790829
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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