A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3563804



Internal ID18418194
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:71112040..71112223hg38UCSC Ensembl
chr1:71577723..71577906hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg38184
hg19184
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9762551
Samples
Known GenesZRANB2-AS2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3563804
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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