A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11229672



Internal ID5908469
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:174359273..174362865hg38UCSC Ensembl
Innerchr3:174359276..174362862hg38UCSC Ensembl
Outerchr3:174359270..174362868hg38UCSC Ensembl
chr3:174077063..174080655hg19UCSC Ensembl
Innerchr3:174077066..174080652hg19UCSC Ensembl
Outerchr3:174077060..174080658hg19UCSC Ensembl
Cytoband3q26.31
Allele length
AssemblyAllele length
hg383593
hg193593
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3598726
Supporting Variants
SamplesNA19321
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11229672
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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