A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637695



Internal ID7024485
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:4346003..4347710hg38UCSC Ensembl
Innerchr16:4346003..4347710hg38UCSC Ensembl
Outerchr16:4345762..4348034hg38UCSC Ensembl
chr16:4396004..4397711hg19UCSC Ensembl
Innerchr16:4396004..4397711hg19UCSC Ensembl
Outerchr16:4395763..4398035hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg381708
hg191708
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15363708
SamplesNA18603
Known GenesCORO7-PAM16, PAM16
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637695
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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