A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25781953



Internal ID19163303
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:215680204..215796690hg38UCSC Ensembl
Innerchr2:216544927..216661413hg19UCSC Ensembl
Innerchr2:216253172..216369658hg18UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg38116487
hg19116487
hg18116487
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893554
Supporting Variants
Samples
Known GenesLINC00607
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=31
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25781953
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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