A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3614636



Internal ID7001529
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:112901192..112905927hg38UCSC Ensembl
Innerchr7:112901196..112905923hg38UCSC Ensembl
Outerchr7:112901188..112905931hg38UCSC Ensembl
chr7:112541247..112545982hg19UCSC Ensembl
Innerchr7:112541251..112545978hg19UCSC Ensembl
Outerchr7:112541243..112545986hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg384736
hg194736
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12931120
SamplesHG01486
Known GenesC7orf60
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3614636
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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