A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3615655



Internal ID7002544
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:156165029..156165921hg38UCSC Ensembl
Innerchr7:156165040..156165910hg38UCSC Ensembl
Outerchr7:156165018..156165932hg38UCSC Ensembl
chr7:155957723..155958615hg19UCSC Ensembl
Innerchr7:155957734..155958604hg19UCSC Ensembl
Outerchr7:155957712..155958626hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg38893
hg19893
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13038337, essv13038343, essv13038336, essv13038342, essv13038341, essv13038338, essv13038340, essv13038339
SamplesHG00315, NA20769, NA20587, NA11840, NA12873, NA20520, NA20792, NA20786
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3615655
Frequency
Sample Size2504
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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