A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15441734



Internal ID5443550
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:29937973..29948907hg38UCSC Ensembl
Innerchr16:29938473..29948407hg38UCSC Ensembl
Outerchr16:29936973..29949907hg38UCSC Ensembl
chr16:29949294..29960228hg19UCSC Ensembl
Innerchr16:29949794..29959728hg19UCSC Ensembl
Outerchr16:29948294..29961228hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg3810935
hg1910935
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3638376
Supporting Variants
SamplesHG03025
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15441734
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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