A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15398510



Internal ID5022107
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3638122
Supporting Variants
SamplesNA18516
Known GenesSYT17
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15398510
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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