A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11360140



Internal ID1307167
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:15672889..15678566hg38UCSC Ensembl
Innerchr4:15672897..15678559hg38UCSC Ensembl
Outerchr4:15672882..15678574hg38UCSC Ensembl
chr4:15674512..15680189hg19UCSC Ensembl
Innerchr4:15674520..15680182hg19UCSC Ensembl
Outerchr4:15674505..15680197hg19UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg385678
hg195678
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3599739
Supporting Variants
SamplesHG01142
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11360140
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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