A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15431200



Internal ID3139541
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:25104681..25105697hg38UCSC Ensembl
Innerchr16:25104681..25105697hg38UCSC Ensembl
Outerchr16:25104488..25105942hg38UCSC Ensembl
chr16:25116002..25117018hg19UCSC Ensembl
Innerchr16:25116002..25117018hg19UCSC Ensembl
Outerchr16:25115809..25117263hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg381017
hg191017
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3638269
Supporting Variants
SamplesHG02768
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15431200
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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