A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15547063



Internal ID5548880
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:84797470..84899017hg38UCSC Ensembl
Innerchr16:84797620..84898867hg38UCSC Ensembl
Outerchr16:84797320..84899167hg38UCSC Ensembl
chr16:84831076..84932623hg19UCSC Ensembl
Innerchr16:84831226..84932473hg19UCSC Ensembl
Outerchr16:84830926..84932773hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg38101548
hg19101548
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3639442
Supporting Variants
SamplesHG02058
Known GenesCRISPLD2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15547063
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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