A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3639177



Internal ID6679272
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:77854701..77926092hg38UCSC Ensembl
Innerchr16:77854724..77926069hg38UCSC Ensembl
Outerchr16:77854678..77926115hg38UCSC Ensembl
chr16:77888598..77959989hg19UCSC Ensembl
Innerchr16:77888621..77959966hg19UCSC Ensembl
Outerchr16:77888575..77960012hg19UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3871392
hg1971392
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15528358
SamplesHG02032
Known GenesVAT1L
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3639177
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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