A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15103651



Internal ID5168491
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:96886602..96897402hg38UCSC Ensembl
Innerchr14:96886612..96897393hg38UCSC Ensembl
Outerchr14:96886593..96897412hg38UCSC Ensembl
chr14:97352939..97363739hg19UCSC Ensembl
Innerchr14:97352949..97363730hg19UCSC Ensembl
Outerchr14:97352930..97363749hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg3810801
hg1910801
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3635430
Supporting Variants
SamplesNA18597
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15103651
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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