A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25783719



Internal ID19169906
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:100392540..100425497hg38UCSC Ensembl
Innerchr10:102152297..102185254hg19UCSC Ensembl
Innerchr10:102142287..102175244hg18UCSC Ensembl
Cytoband10q24.31
Allele length
AssemblyAllele length
hg3832958
hg1932958
hg1832958
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891888
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=11
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25783719
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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