A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2662662



Internal ID9928767
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:88419048..88430779hg38UCSC Ensembl
Outerchr3:88418891..88430932hg38UCSC Ensembl
Innerchr3:88468198..88479929hg19UCSC Ensembl
Outerchr3:88468041..88480082hg19UCSC Ensembl
Cytoband3p11.1
Allele length
AssemblyAllele length
hg3812042
hg1912042
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv869e199
Supporting Variantsessv5497020, essv6309858, essv6136396
SamplesHG00537, HG00684, NA19003
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2662662
Frequency
Sample Size1151
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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