A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25796625



Internal ID19178440
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:72410114..72425880hg38UCSC Ensembl
Innerchr10:74169872..74185638hg19UCSC Ensembl
Innerchr10:73839878..73855644hg18UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg3815767
hg1915767
hg1815767
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891858
Supporting Variants
Samples
Known GenesMICU1, MIR1256
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=6
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25796625
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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