A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3614130



Internal ID7001025
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:91857444..91883636hg38UCSC Ensembl
Innerchr7:91857444..91883636hg38UCSC Ensembl
Outerchr7:91856944..91884136hg38UCSC Ensembl
chr7:91486758..91512950hg19UCSC Ensembl
Innerchr7:91486758..91512950hg19UCSC Ensembl
Outerchr7:91486258..91513450hg19UCSC Ensembl
Cytoband7q21.2
Allele length
AssemblyAllele length
hg3826193
hg1926193
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12889141
SamplesHG02084
Known GenesMTERF
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3614130
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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