A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25792412



Internal ID19165914
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:96311049..96403228hg38UCSC Ensembl
Innerchr6:96758925..96851104hg19UCSC Ensembl
Innerchr6:96865646..96957825hg18UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg3892180
hg1992180
hg1892180
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3890913
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=21
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25792412
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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