A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5396345



Internal ID9088856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:160944086..160949414hg38UCSC Ensembl
Outerchr3:160943929..160949567hg38UCSC Ensembl
Innerchr3:160661874..160667202hg19UCSC Ensembl
Outerchr3:160661717..160667355hg19UCSC Ensembl
Cytoband3q25.33
Allele length
AssemblyAllele length
hg385639
hg195639
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2665188
Supporting Variants
SamplesHG01069
Known GenesPPM1L
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5396345
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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