A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3615654



Internal ID7002543
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:156148003..156152818hg38UCSC Ensembl
Innerchr7:156148036..156152785hg38UCSC Ensembl
Outerchr7:156147970..156152851hg38UCSC Ensembl
chr7:155940697..155945512hg19UCSC Ensembl
Innerchr7:155940730..155945479hg19UCSC Ensembl
Outerchr7:155940664..155945545hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg384816
hg194816
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13038335
SamplesHG02215
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3615654
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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