A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15359785



Internal ID4370327
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:1357700..1359042hg38UCSC Ensembl
Innerchr16:1357704..1359039hg38UCSC Ensembl
Outerchr16:1357697..1359046hg38UCSC Ensembl
chr16:1407701..1409043hg19UCSC Ensembl
Innerchr16:1407705..1409040hg19UCSC Ensembl
Outerchr16:1407698..1409047hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg381343
hg191343
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3637617
Supporting Variants
SamplesHG03899
Known GenesGNPTG
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15359785
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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