A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3638269



Internal ID7025055
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15431200, essv15431202, essv15431198, essv15431206, essv15431208, essv15431197, essv15431207, essv15431199, essv15431201, essv15431205, essv15431203, essv15431204
SamplesHG02811, HG03135, HG02756, NA19901, NA19200, HG02757, NA18856, HG02675, NA19117, NA19713, HG02768, NA19096
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3638269
Frequency
Sample Size2504
Observed Gain0
Observed Loss12
Observed Complex0
Frequencyn/a


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