A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637788



Internal ID6677889
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:7012017..7032782hg38UCSC Ensembl
Innerchr16:7012017..7032782hg38UCSC Ensembl
Outerchr16:7011777..7033022hg38UCSC Ensembl
chr16:7062018..7082783hg19UCSC Ensembl
Innerchr16:7062018..7082783hg19UCSC Ensembl
Outerchr16:7061778..7083023hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3820766
hg1920766
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15365826, essv15365823, essv15365829, essv15365825, essv15365828, essv15365827, essv15365824
SamplesNA19011, NA18593, NA19091, HG03237, HG00311, NA18574, HG00684
Known GenesRBFOX1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637788
Frequency
Sample Size2504
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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