A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6394171



Internal ID9502073
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:35306479..35307509hg38UCSC Ensembl
chr14:35775685..35776715hg19UCSC Ensembl
Cytoband14q13.2
Allele length
AssemblyAllele length
hg381031
hg191031
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2661597
Supporting Variants
SamplesNA18982
Known GenesPSMA6
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6394171
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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