A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3639355



Internal ID7026137
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:82149872..82196025hg38UCSC Ensembl
Innerchr16:82149889..82196009hg38UCSC Ensembl
Outerchr16:82149856..82196042hg38UCSC Ensembl
chr16:82183477..82229630hg19UCSC Ensembl
Innerchr16:82183494..82229614hg19UCSC Ensembl
Outerchr16:82183461..82229647hg19UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg3846154
hg1946154
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15542310
SamplesHG03607
Known GenesMPHOSPH6
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3639355
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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