A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25781617



Internal ID18833217
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:46766277..46802757hg38UCSC Ensembl
Innerchr3:46807767..46844247hg19UCSC Ensembl
Innerchr3:46782771..46819251hg18UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg3836481
hg1936481
hg1836481
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893692
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=6
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25781617
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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