A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3597039



Internal ID6984353
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:95063569..95068105hg38UCSC Ensembl
Innerchr3:95063572..95068103hg38UCSC Ensembl
Outerchr3:95063567..95068108hg38UCSC Ensembl
chr3:94782413..94786949hg19UCSC Ensembl
Innerchr3:94782416..94786947hg19UCSC Ensembl
Outerchr3:94782411..94786952hg19UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg384537
hg194537
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11070081, essv11070085, essv11070087, essv11070077, essv11070088, essv11070078, essv11070083, essv11070090, essv11070084, essv11070079, essv11070089, essv11070080, essv11070082, essv11070086, essv11070076
SamplesHG01850, HG02061, HG01809, HG02156, HG02521, HG01843, HG02513, HG02380, HG02127, HG03934, HG01812, HG03916, HG02028, HG04153, HG01805
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3597039
Frequency
Sample Size2504
Observed Gain0
Observed Loss15
Observed Complex0
Frequencyn/a


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