A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15537864



Internal ID3374105
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:81636931..81642472hg38UCSC Ensembl
Innerchr16:81636948..81642456hg38UCSC Ensembl
Outerchr16:81636915..81642489hg38UCSC Ensembl
chr16:81670536..81676077hg19UCSC Ensembl
Innerchr16:81670553..81676061hg19UCSC Ensembl
Outerchr16:81670520..81676094hg19UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg385542
hg195542
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3639337
Supporting Variants
SamplesHG03022
Known GenesCMIP
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15537864
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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