A curated catalogue of human genomic structural variation




Variant Details

Variant: essv10893453



Internal ID1841792
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:241325760..241335933hg38UCSC Ensembl
chr2:242265175..242275348hg19UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg3810174
hg1910174
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3594827
Supporting Variants
SamplesHG01708
Known GenesSEPT2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv10893453
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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