A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15566680



Internal ID5568496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:88495541..88499018hg38UCSC Ensembl
Innerchr16:88495541..88499018hg38UCSC Ensembl
Outerchr16:88495259..88499198hg38UCSC Ensembl
chr16:88561949..88565426hg19UCSC Ensembl
Innerchr16:88561949..88565426hg19UCSC Ensembl
Outerchr16:88561667..88565606hg19UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg383478
hg193478
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3639549
Supporting Variants
SamplesNA19079
Known GenesZFPM1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15566680
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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