A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3612405



Internal ID6999306
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:16859996..16877613hg38UCSC Ensembl
Innerchr7:16860032..16877577hg38UCSC Ensembl
Outerchr7:16859960..16877649hg38UCSC Ensembl
chr7:16899620..16917237hg19UCSC Ensembl
Innerchr7:16899656..16917201hg19UCSC Ensembl
Outerchr7:16899584..16917273hg19UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg3817618
hg1917618
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12688306, essv12688308, essv12688307, essv12688310, essv12688309
SamplesHG04158, HG02691, NA20513, HG03006, HG03872
Known GenesAGR3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3612405
Frequency
Sample Size2504
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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