A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25779350



Internal ID18835999
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:31819853..31827305hg38UCSC Ensembl
Innerchr6:31787630..31795082hg19UCSC Ensembl
Innerchr6:31895609..31903061hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg387453
hg197453
hg187453
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3890822
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=12
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25779350
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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