A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3594155



Internal ID6634431
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:210367742..210374045hg38UCSC Ensembl
Innerchr2:210367742..210374045hg38UCSC Ensembl
Outerchr2:210367539..210374255hg38UCSC Ensembl
chr2:211232466..211238769hg19UCSC Ensembl
Innerchr2:211232466..211238769hg19UCSC Ensembl
Outerchr2:211232263..211238979hg19UCSC Ensembl
Cytoband2q34
Allele length
AssemblyAllele length
hg386304
hg196304
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10835430
SamplesHG01440
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3594155
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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