A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3614136



Internal ID7001031
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:92143541..92148116hg38UCSC Ensembl
Innerchr7:92143541..92148116hg38UCSC Ensembl
Outerchr7:92143370..92148187hg38UCSC Ensembl
chr7:91772855..91777430hg19UCSC Ensembl
Innerchr7:91772855..91777430hg19UCSC Ensembl
Outerchr7:91772684..91777501hg19UCSC Ensembl
Cytoband7q21.2
Allele length
AssemblyAllele length
hg384576
hg194576
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12890519
SamplesNA19256
Known GenesLRRD1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3614136
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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