A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3375555



Internal ID15222530
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:156013069..156013097hg38UCSC Ensembl
Innerchr7:156013067..156013097hg38UCSC Ensembl
Outerchr7:156013039..156013127hg38UCSC Ensembl
chr7:155805763..155805791hg19UCSC Ensembl
Innerchr7:155805761..155805791hg19UCSC Ensembl
Outerchr7:155805733..155805821hg19UCSC Ensembl
chr7:155498524..155498552hg18UCSC Ensembl
Innerchr7:155498552..155498522hg18UCSC Ensembl
Outerchr7:155498494..155498582hg18UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg38277
hg19277
hg18277
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8938109, essv8938105, essv8938106, essv8938107, essv8938108
SamplesNA19172, NA18520, NA19114, NA19108, NA18517
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3375555
Frequency
Sample Size185
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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