A curated catalogue of human genomic structural variation




Variant Details

Variant: essv10896252



Internal ID3103484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:71733..171693hg38UCSC Ensembl
Innerchr3:71883..171543hg38UCSC Ensembl
Outerchr3:71583..171843hg38UCSC Ensembl
chr3:113416..213376hg19UCSC Ensembl
Innerchr3:113566..213226hg19UCSC Ensembl
Outerchr3:113266..213526hg19UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg3899961
hg1999961
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3594880
Supporting Variants
SamplesHG02725
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv10896252
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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