A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3639334



Internal ID6679429
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:81431663..81475655hg38UCSC Ensembl
Innerchr16:81431663..81475655hg38UCSC Ensembl
Outerchr16:81431163..81476155hg38UCSC Ensembl
chr16:81465268..81509260hg19UCSC Ensembl
Innerchr16:81465268..81509260hg19UCSC Ensembl
Outerchr16:81464768..81509760hg19UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg3843993
hg1943993
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15537859
SamplesHG02661
Known GenesCMIP
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3639334
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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