A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3614044



Internal ID6654251
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:87978760..87988904hg38UCSC Ensembl
Innerchr7:87978786..87988878hg38UCSC Ensembl
Outerchr7:87978734..87988930hg38UCSC Ensembl
chr7:87608075..87618219hg19UCSC Ensembl
Innerchr7:87608101..87618193hg19UCSC Ensembl
Outerchr7:87608049..87618245hg19UCSC Ensembl
Cytoband7q21.12
Allele length
AssemblyAllele length
hg3810145
hg1910145
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12879851, essv12879854, essv12879853, essv12879852, essv12879855, essv12879856
SamplesNA19031, HG03380, HG03470, HG02054, HG03455, HG03168
Known GenesADAM22
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3614044
Frequency
Sample Size2504
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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