A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15103710



Internal ID6808299
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:97386032..97386847hg38UCSC Ensembl
Innerchr14:97386044..97386836hg38UCSC Ensembl
Outerchr14:97386021..97386859hg38UCSC Ensembl
chr14:97852369..97853184hg19UCSC Ensembl
Innerchr14:97852381..97853173hg19UCSC Ensembl
Outerchr14:97852358..97853196hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg38816
hg19816
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3635440
Supporting Variants
SamplesNA20894
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15103710
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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