A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15537859



Internal ID5539675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:81431663..81475655hg38UCSC Ensembl
Innerchr16:81431663..81475655hg38UCSC Ensembl
Outerchr16:81431163..81476155hg38UCSC Ensembl
chr16:81465268..81509260hg19UCSC Ensembl
Innerchr16:81465268..81509260hg19UCSC Ensembl
Outerchr16:81464768..81509760hg19UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg3843993
hg1943993
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3639334
Supporting Variants
SamplesHG02661
Known GenesCMIP
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15537859
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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