A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25799994



Internal ID18826343
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:29900276..29925263hg38UCSC Ensembl
Innerchr6:29868053..29893040hg19UCSC Ensembl
Innerchr6:29976032..30001019hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3824988
hg1924988
hg1824988
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3890806
Supporting Variants
Samples
Known GenesHCG4B
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=29
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25799994
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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