A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25800501



Internal ID19179419
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:7016730..7094901hg38UCSC Ensembl
Innerchr3:7058417..7136588hg19UCSC Ensembl
Innerchr3:7033417..7111588hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3878172
hg1978172
hg1878172
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893653
Supporting Variants
Samples
Known GenesGRM7
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=38
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25800501
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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