A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11394156



Internal ID5390003
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:35653589..35660343hg38UCSC Ensembl
Innerchr4:35653600..35660332hg38UCSC Ensembl
Outerchr4:35653578..35660354hg38UCSC Ensembl
chr4:35655211..35661965hg19UCSC Ensembl
Innerchr4:35655222..35661954hg19UCSC Ensembl
Outerchr4:35655200..35661976hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg386755
hg196755
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3600198
Supporting Variants
SamplesNA18939
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11394156
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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