A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15566683



Internal ID5568499
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:88504858..88538312hg38UCSC Ensembl
chr16:88571266..88604720hg19UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg3833455
hg1933455
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3639551
Supporting Variants
SamplesHG03457
Known GenesZFPM1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15566683
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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