A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3639101



Internal ID6679196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:75599180..75622670hg38UCSC Ensembl
Innerchr16:75599180..75622670hg38UCSC Ensembl
Outerchr16:75598680..75623170hg38UCSC Ensembl
chr16:75633078..75656568hg19UCSC Ensembl
Innerchr16:75633078..75656568hg19UCSC Ensembl
Outerchr16:75632578..75657068hg19UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3823491
hg1923491
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15523487
SamplesHG02491
Known GenesADAT1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3639101
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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