A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637655



Internal ID7024445
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:3179097..3198941hg38UCSC Ensembl
Innerchr16:3179125..3198913hg38UCSC Ensembl
Outerchr16:3179069..3198969hg38UCSC Ensembl
chr16:3229098..3248941hg19UCSC Ensembl
Innerchr16:3229126..3248913hg19UCSC Ensembl
Outerchr16:3229070..3248969hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3819845
hg1919844
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15362874
SamplesHG02384
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637655
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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