A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15566681



Internal ID5568497
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:88495809..88498218hg38UCSC Ensembl
Innerchr16:88495809..88498218hg38UCSC Ensembl
Outerchr16:88495701..88498466hg38UCSC Ensembl
chr16:88562217..88564626hg19UCSC Ensembl
Innerchr16:88562217..88564626hg19UCSC Ensembl
Outerchr16:88562109..88564874hg19UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg382410
hg192410
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3639550
Supporting Variants
SamplesNA18907
Known GenesZFPM1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15566681
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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