A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15103560



Internal ID5105376
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:96364866..96366338hg38UCSC Ensembl
Innerchr14:96364877..96366328hg38UCSC Ensembl
Outerchr14:96364856..96366349hg38UCSC Ensembl
chr14:96831203..96832675hg19UCSC Ensembl
Innerchr14:96831214..96832665hg19UCSC Ensembl
Outerchr14:96831193..96832686hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg381473
hg191473
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3635422
Supporting Variants
SamplesHG02266
Known GenesGSKIP
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15103560
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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