A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9908804



Internal ID5908861
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:37077711..37093365hg38UCSC Ensembl
chr1:37543312..37558966hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg3815655
hg1915655
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3585745
Supporting Variants
SamplesNA19321
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv9908804
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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