A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15089815



Internal ID6604644
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:85738866..85777730hg38UCSC Ensembl
Innerchr14:85738866..85777730hg38UCSC Ensembl
Outerchr14:85738366..85778230hg38UCSC Ensembl
chr14:86205210..86244074hg19UCSC Ensembl
Innerchr14:86205210..86244074hg19UCSC Ensembl
Outerchr14:86204710..86244574hg19UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg3838865
hg1938865
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3635203
Supporting Variants
SamplesNA20773
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15089815
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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