A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25800932



Internal ID18829963
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:10513722..10531953hg38UCSC Ensembl
Innerchr6:10513955..10532186hg19UCSC Ensembl
Innerchr6:10621941..10640172hg18UCSC Ensembl
Cytoband6p24.2
Allele length
AssemblyAllele length
hg3818232
hg1918232
hg1818232
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3890790
Supporting Variants
Samples
Known GenesGCNT2
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=10
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25800932
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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