A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6502929



Internal ID20876178
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:96539972..96540552hg38UCSC Ensembl
chr14:97006309..97006889hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg38581
hg19581
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18022457
Samples
Known GenesPAPOLA
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6502929
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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