A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25780864



Internal ID18818149
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:82171786..82294496hg38UCSC Ensembl
Innerchr10:83931542..84054252hg19UCSC Ensembl
Innerchr10:83921522..84044232hg18UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg38122711
hg19122711
hg18122711
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891875
Supporting Variants
Samples
Known GenesNRG3
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=50
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25780864
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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