A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3614448



Internal ID7001342
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:106669950..106681873hg38UCSC Ensembl
Innerchr7:106669970..106681853hg38UCSC Ensembl
Outerchr7:106669930..106681893hg38UCSC Ensembl
chr7:106310396..106322319hg19UCSC Ensembl
Innerchr7:106310416..106322299hg19UCSC Ensembl
Outerchr7:106310376..106322339hg19UCSC Ensembl
Cytoband7q22.3
Allele length
AssemblyAllele length
hg3811924
hg1911924
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12917661
SamplesNA20846
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3614448
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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