A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891808



Internal ID18839518
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:50479472..50531848hg38UCSC Ensembl
Outerchr10:50479472..50531848hg38UCSC Ensembl
Innerchr10:52239232..52291608hg19UCSC Ensembl
Outerchr10:52239232..52291608hg19UCSC Ensembl
Innerchr10:51909238..51961614hg18UCSC Ensembl
Outerchr10:51909238..51961614hg18UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg3852377
hg1952377
hg1852377
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25787644, essv25779105
Samples
Known GenesSGMS1
MethodSNP array
Analysis
PlatformIllumina HumanHap 550
Illumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891808
Frequency
Sample Size3017
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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