A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3638080



Internal ID6678178
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:17458968..17460092hg38UCSC Ensembl
Innerchr16:17459020..17460041hg38UCSC Ensembl
Outerchr16:17458917..17460144hg38UCSC Ensembl
chr16:17552825..17553949hg19UCSC Ensembl
Innerchr16:17552877..17553898hg19UCSC Ensembl
Outerchr16:17552774..17554001hg19UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg381125
hg191125
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15391008
SamplesNA18559
Known GenesXYLT1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3638080
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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