A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3597176



Internal ID6637446
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:100605159..100610785hg38UCSC Ensembl
Innerchr3:100605159..100610785hg38UCSC Ensembl
Outerchr3:100605065..100610843hg38UCSC Ensembl
chr3:100324003..100329629hg19UCSC Ensembl
Innerchr3:100324003..100329629hg19UCSC Ensembl
Outerchr3:100323909..100329687hg19UCSC Ensembl
Cytoband3q12.2
Allele length
AssemblyAllele length
hg385627
hg195627
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11085808
SamplesNA18552
Known GenesGPR128
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3597176
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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