A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15372774



Internal ID1289407
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:9292915..9318147hg38UCSC Ensembl
Innerchr16:9292965..9318097hg38UCSC Ensembl
Outerchr16:9292855..9318207hg38UCSC Ensembl
chr16:9386772..9412004hg19UCSC Ensembl
Innerchr16:9386822..9411954hg19UCSC Ensembl
Outerchr16:9386712..9412064hg19UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg3825233
hg1925233
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3637870
Supporting Variants
SamplesHG01133
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15372774
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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