A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637649



Internal ID7024440
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:3069789..3083133hg38UCSC Ensembl
Innerchr16:3070289..3082633hg38UCSC Ensembl
Outerchr16:3068789..3084133hg38UCSC Ensembl
chr16:3119790..3133134hg19UCSC Ensembl
Innerchr16:3120290..3132634hg19UCSC Ensembl
Outerchr16:3118790..3134134hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3813345
hg1913345
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv474e214
Supporting Variantsessv15362849, essv15362852, essv15362851, essv15362850, essv15362848, essv15362853
SamplesHG01965, NA20808, NA12748, HG01512, HG01342, NA20510
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637649
Frequency
Sample Size2504
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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