A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13501248



Internal ID6032780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:63758397..63792702hg38UCSC Ensembl
chr9:68354131..68388436hg19UCSC Ensembl
Cytoband9q13
Allele length
AssemblyAllele length
hg3834306
hg1934306
Variant TypeCNV gain
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3620531
Supporting Variants
SamplesNA19438
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13501248
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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