A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15537869



Internal ID5539685
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:81696019..81869162hg38UCSC Ensembl
chr16:81729624..81902767hg19UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg38173144
hg19173144
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3639339
Supporting Variants
SamplesHG02661
Known GenesCMIP, PLCG2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15537869
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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