A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3595396



Internal ID6982714
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:16003311..16010600hg38UCSC Ensembl
Innerchr3:16003316..16010595hg38UCSC Ensembl
Outerchr3:16003306..16010605hg38UCSC Ensembl
chr3:16044818..16052107hg19UCSC Ensembl
Innerchr3:16044823..16052102hg19UCSC Ensembl
Outerchr3:16044813..16052112hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg387290
hg197290
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10937256
SamplesHG01414
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3595396
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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