A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3615653



Internal ID7002542
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:156145763..156147564hg38UCSC Ensembl
Innerchr7:156145790..156147537hg38UCSC Ensembl
Outerchr7:156145736..156147591hg38UCSC Ensembl
chr7:155938457..155940258hg19UCSC Ensembl
Innerchr7:155938484..155940231hg19UCSC Ensembl
Outerchr7:155938430..155940285hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg381802
hg191802
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13038334
SamplesHG02215
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3615653
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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