A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637663



Internal ID7024453
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:3344547..3345314hg38UCSC Ensembl
Innerchr16:3344604..3345257hg38UCSC Ensembl
Outerchr16:3344490..3345371hg38UCSC Ensembl
chr16:3394547..3395314hg19UCSC Ensembl
Innerchr16:3394604..3395257hg19UCSC Ensembl
Outerchr16:3394490..3395371hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38768
hg19768
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15362980, essv15362977, essv15362982, essv15362985, essv15362979, essv15362978, essv15362983, essv15362981, essv15362984
SamplesHG01860, HG02016, HG02140, HG03830, HG02131, HG01844, HG00463, HG02351, HG00978
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637663
Frequency
Sample Size2504
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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