A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637906



Internal ID6678006
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:10527553..10532502hg38UCSC Ensembl
Innerchr16:10527553..10532502hg38UCSC Ensembl
Outerchr16:10527267..10532774hg38UCSC Ensembl
chr16:10621410..10626359hg19UCSC Ensembl
Innerchr16:10621410..10626359hg19UCSC Ensembl
Outerchr16:10621124..10626631hg19UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg384950
hg194950
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15373031, essv15373032, essv15373033
SamplesHG00662, HG00620, HG00560
Known GenesEMP2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637906
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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