A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6538303



Internal ID9515706
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:141915074..141915477hg38UCSC Ensembl
Outerchr3:141915037..141915527hg38UCSC Ensembl
Innerchr3:141633916..141634319hg19UCSC Ensembl
Outerchr3:141633879..141634369hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg38491
hg19491
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2656624
Supporting Variants
SamplesHG00421
Known GenesATP1B3
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6538303
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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