A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3326760



Internal ID15173743
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:170467634..170467664hg38UCSC Ensembl
Innerchr4:170467636..170467659hg38UCSC Ensembl
Outerchr4:170467606..170467689hg38UCSC Ensembl
chr4:171388785..171388815hg19UCSC Ensembl
Innerchr4:171388787..171388810hg19UCSC Ensembl
Outerchr4:171388757..171388840hg19UCSC Ensembl
chr4:171625360..171625390hg18UCSC Ensembl
Innerchr4:171625385..171625362hg18UCSC Ensembl
Outerchr4:171625332..171625415hg18UCSC Ensembl
Cytoband4q33
Allele length
AssemblyAllele length
hg38237
hg19237
hg18237
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8675484
SamplesNA12892
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3326760
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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