A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3596934



Internal ID6984248
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:88627902..88632477hg38UCSC Ensembl
Innerchr3:88627902..88632477hg38UCSC Ensembl
Outerchr3:88627784..88632529hg38UCSC Ensembl
chr3:88677052..88681627hg19UCSC Ensembl
Innerchr3:88677052..88681627hg19UCSC Ensembl
Outerchr3:88676934..88681679hg19UCSC Ensembl
Cytoband3p11.1
Allele length
AssemblyAllele length
hg384576
hg194576
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11067993
SamplesHG02286
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3596934
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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