A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25800673



Internal ID19173748
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:6612823..6620173hg38UCSC Ensembl
Innerchr10:6654785..6662135hg19UCSC Ensembl
Innerchr10:6694791..6702141hg18UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg387351
hg197351
hg187351
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891746
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=5
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25800673
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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