A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25787055



Internal ID19175162
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:156958723..156991616hg38UCSC Ensembl
Innerchr6:157279857..157312750hg19UCSC Ensembl
Innerchr6:157321549..157354442hg18UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg3832894
hg1932894
hg1832894
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3890969
Supporting Variants
Samples
Known GenesARID1B
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=8
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25787055
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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