A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15060892



Internal ID4433656
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:73968884..73993503hg38UCSC Ensembl
chr14:74435587..74460206hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg3824620
hg1924620
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3634927
Supporting Variants
SamplesHG03945
Known GenesENTPD5
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15060892
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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