A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3634994



Internal ID7021794
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:76955561..76957277hg38UCSC Ensembl
Innerchr14:76955566..76957272hg38UCSC Ensembl
Outerchr14:76955556..76957282hg38UCSC Ensembl
chr14:77421904..77423620hg19UCSC Ensembl
Innerchr14:77421909..77423615hg19UCSC Ensembl
Outerchr14:77421899..77423625hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg381717
hg191717
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15068983, essv15068982
SamplesHG02282, NA19146
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3634994
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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