A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3615246



Internal ID7002135
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:140993522..140995286hg38UCSC Ensembl
Innerchr7:140993530..140995279hg38UCSC Ensembl
Outerchr7:140993515..140995294hg38UCSC Ensembl
chr7:140693322..140695086hg19UCSC Ensembl
Innerchr7:140693330..140695079hg19UCSC Ensembl
Outerchr7:140693315..140695094hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg381765
hg191765
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12985096
SamplesHG00732
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3615246
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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