A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3890880



Internal ID18838496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:75364726..75498207hg38UCSC Ensembl
Outerchr6:75364726..75498207hg38UCSC Ensembl
Innerchr6:76074442..76207923hg19UCSC Ensembl
Outerchr6:76074442..76207923hg19UCSC Ensembl
Innerchr6:76131162..76264643hg18UCSC Ensembl
Outerchr6:76131162..76264643hg18UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg38133482
hg19133482
hg18133482
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25799505
Samples
Known GenesFILIP1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3890880
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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