A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3638122



Internal ID7024908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:19240862..19251562hg38UCSC Ensembl
Innerchr16:19240862..19251562hg38UCSC Ensembl
Outerchr16:19240362..19252062hg38UCSC Ensembl
chr16:19252184..19262884hg19UCSC Ensembl
Innerchr16:19252184..19262884hg19UCSC Ensembl
Outerchr16:19251684..19263384hg19UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg3810701
hg1910701
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15398510
SamplesNA18516
Known GenesSYT17
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3638122
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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