A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3614156



Internal ID7001051
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:93163904..93167560hg38UCSC Ensembl
Innerchr7:93163943..93167521hg38UCSC Ensembl
Outerchr7:93163865..93167599hg38UCSC Ensembl
chr7:92793217..92796873hg19UCSC Ensembl
Innerchr7:92793256..92796834hg19UCSC Ensembl
Outerchr7:92793178..92796912hg19UCSC Ensembl
Cytoband7q21.2
Allele length
AssemblyAllele length
hg383657
hg193657
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12890772
SamplesHG03884
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3614156
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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