A curated catalogue of human genomic structural variation




Variant Details

Variant: essv10834504



Internal ID1925754
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:209131573..209167268hg38UCSC Ensembl
chr2:209996297..210031992hg19UCSC Ensembl
Cytoband2q34
Allele length
AssemblyAllele length
hg3835696
hg1935696
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3594138
Supporting Variants
SamplesHG01798
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv10834504
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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