A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3595689



Internal ID6983007
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:28470104..28495655hg38UCSC Ensembl
Innerchr3:28470120..28495639hg38UCSC Ensembl
Outerchr3:28470088..28495671hg38UCSC Ensembl
chr3:28511595..28537146hg19UCSC Ensembl
Innerchr3:28511611..28537130hg19UCSC Ensembl
Outerchr3:28511579..28537162hg19UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg3825552
hg1925552
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10964591
SamplesHG04239
Known GenesZCWPW2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3595689
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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