A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15114738



Internal ID5461557
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:104619697..104631319hg38UCSC Ensembl
Innerchr14:104620197..104630819hg38UCSC Ensembl
Outerchr14:104618697..104632319hg38UCSC Ensembl
chr14:105086034..105097656hg19UCSC Ensembl
Innerchr14:105086534..105097156hg19UCSC Ensembl
Outerchr14:105085034..105098656hg19UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg3811623
hg1911623
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3635624
Supporting Variants
SamplesNA18969
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15114738
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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