A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14333831



Internal ID4335647
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:1472405..1478533hg38UCSC Ensembl
Innerchr12:1472455..1478483hg38UCSC Ensembl
Outerchr12:1472317..1478621hg38UCSC Ensembl
chr12:1581571..1587699hg19UCSC Ensembl
Innerchr12:1581621..1587649hg19UCSC Ensembl
Outerchr12:1581483..1587787hg19UCSC Ensembl
Cytoband12p13.33
Allele length
AssemblyAllele length
hg386129
hg196129
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3628284
Supporting Variants
SamplesNA20876
Known GenesERC1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14333831
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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