A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637700



Internal ID7024490
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:4712146..4713029hg38UCSC Ensembl
Innerchr16:4712146..4713029hg38UCSC Ensembl
Outerchr16:4711819..4713350hg38UCSC Ensembl
chr16:4762147..4763030hg19UCSC Ensembl
Innerchr16:4762147..4763030hg19UCSC Ensembl
Outerchr16:4761820..4763351hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38884
hg19884
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15363721, essv15363725, essv15363722, essv15363719, essv15363727, essv15363723, essv15363728, essv15363718, essv15363724, essv15363726, essv15363720
SamplesHG03366, HG03378, HG03130, HG03436, NA19315, NA20320, NA19347, HG03575, NA18876, HG01914, HG03265
Known GenesANKS3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637700
Frequency
Sample Size2504
Observed Gain0
Observed Loss11
Observed Complex0
Frequencyn/a


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