A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15103426



Internal ID2833721
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:96061027..96069365hg38UCSC Ensembl
Innerchr14:96061028..96069365hg38UCSC Ensembl
Outerchr14:96061027..96069366hg38UCSC Ensembl
chr14:96527364..96535702hg19UCSC Ensembl
Innerchr14:96527365..96535702hg19UCSC Ensembl
Outerchr14:96527364..96535703hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg388339
hg198339
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3635413
Supporting Variants
SamplesHG02497
Known GenesC14orf132
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15103426
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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