A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6499528



Internal ID20872749
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:94449342..94458377hg38UCSC Ensembl
chr14:94915679..94924714hg19UCSC Ensembl
Cytoband14q32.13
Allele length
AssemblyAllele length
hg389036
hg199036
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18022936
Samples
Known GenesSERPINA11
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6499528
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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