A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14868839



Internal ID4870655
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:95185612..95186267hg38UCSC Ensembl
Innerchr13:95185618..95186262hg38UCSC Ensembl
Outerchr13:95185607..95186273hg38UCSC Ensembl
chr13:95837866..95838521hg19UCSC Ensembl
Innerchr13:95837872..95838516hg19UCSC Ensembl
Outerchr13:95837861..95838527hg19UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg38656
hg19656
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3633240
Supporting Variants
SamplesHG03061
Known GenesABCC4
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14868839
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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