A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637954



Internal ID7024741
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:12086299..12113970hg38UCSC Ensembl
Innerchr16:12086299..12113970hg38UCSC Ensembl
Outerchr16:12085799..12114470hg38UCSC Ensembl
chr16:12180156..12207827hg19UCSC Ensembl
Innerchr16:12180156..12207827hg19UCSC Ensembl
Outerchr16:12179656..12208327hg19UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg3827672
hg1927672
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15377345
SamplesHG04094
Known GenesSNX29
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637954
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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