A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25799042



Internal ID19174705
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:6673465..6739489hg38UCSC Ensembl
Innerchr9:6673465..6739489hg19UCSC Ensembl
Innerchr9:6663465..6729489hg18UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg3866025
hg1966025
hg1866025
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891542
Supporting Variants
Samples
Known GenesKDM4C
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=20
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25799042
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