A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893554



Internal ID19184374
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:215680204..215796690hg38UCSC Ensembl
Outerchr2:215680204..215796690hg38UCSC Ensembl
Innerchr2:216544927..216661413hg19UCSC Ensembl
Outerchr2:216544927..216661413hg19UCSC Ensembl
Innerchr2:216253172..216369658hg18UCSC Ensembl
Outerchr2:216253172..216369658hg18UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg38116487
hg19116487
hg18116487
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25781953
Samples
Known GenesLINC00607
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893554
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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