A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6497991



Internal ID20871199
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:92523401..92529499hg38UCSC Ensembl
chr14:92989745..92995843hg19UCSC Ensembl
Cytoband14q32.12
Allele length
AssemblyAllele length
hg386099
hg196099
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18021827
Samples
Known GenesRIN3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6497991
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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