A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25779105



Internal ID18821291
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:50479472..50531848hg38UCSC Ensembl
Innerchr10:52239232..52291608hg19UCSC Ensembl
Innerchr10:51909238..51961614hg18UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg3852377
hg1952377
hg1852377
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891808
Supporting Variants
Samples
Known GenesSGMS1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=15
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25779105
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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