A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3596644



Internal ID6983958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:76673696..76755760hg38UCSC Ensembl
Innerchr3:76673723..76755733hg38UCSC Ensembl
Outerchr3:76673669..76755787hg38UCSC Ensembl
chr3:76722847..76804911hg19UCSC Ensembl
Innerchr3:76722874..76804884hg19UCSC Ensembl
Outerchr3:76722820..76804938hg19UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg3882065
hg1982065
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv903e214
Supporting Variantsessv11047187
SamplesHG03240
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3596644
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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