A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3638324



Internal ID6678422
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:27325118..27339932hg38UCSC Ensembl
Innerchr16:27325118..27339932hg38UCSC Ensembl
Outerchr16:27324870..27340223hg38UCSC Ensembl
chr16:27336439..27351253hg19UCSC Ensembl
Innerchr16:27336439..27351253hg19UCSC Ensembl
Outerchr16:27336191..27351544hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg3814815
hg1914815
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15439413, essv15439418, essv15439415, essv15439417, essv15439414, essv15439412, essv15439411, essv15439410, essv15439419, essv15439416
SamplesHG01089, HG00112, HG00117, HG03488, NA12004, HG01670, HG02235, HG00324, HG00143, HG00336
Known GenesIL4R
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3638324
Frequency
Sample Size2504
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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