A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6033097



Internal ID21942440
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:61688417..61718006hg38UCSC Ensembl
chr14:62155135..62184724hg19UCSC Ensembl
Cytoband14q23.2
Allele length
AssemblyAllele length
hg3829590
hg1929590
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17603755
Samples
Known GenesHIF1A, HIF1A-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6033097
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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