A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15107088



Internal ID6070269
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:99605006..99658124hg38UCSC Ensembl
chr14:100071343..100124461hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg3853119
hg1953119
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3635486
Supporting Variants
SamplesNA19457
Known GenesHHIPL1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15107088
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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